UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, DCD.C. 20549
 
FORM 10-Q
 
(Mark One)
QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the quarterly period ended March 31, 20232024
or
TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the transition period from              to             
COMMISSION FILE NO.NUMBER 000-26224
 
INTEGRA LIFESCIENCES HOLDINGS CORPORATION
(EXACT NAME OF REGISTRANT AS SPECIFIED IN ITS CHARTER)
 
Delaware 51-0317849
(STATE OR OTHER JURISDICTION OF
INCORPORATION OR ORGANIZATION)
 (I.R.S. EMPLOYER
IDENTIFICATION NO.)
1100 Campus Road 08540
Princeton,New Jersey(ZIP CODE)
(ADDRESS OF PRINCIPAL EXECUTIVE OFFICES) 
Registrant's Telephone Number, Including Area Code: (609) 275-0500
Former Name, Former Address and Former Fiscal Year, if Changed Since Last Report:
Securities registered pursuant to Section 12(b) of the Act:
TITLE OF EACH CLASSTRADING SYMBOLNAME OF EACH EXCHANGE ON WHICH REGISTERED
Common Stock, Par Value $.01 Per ShareIARTNasdaq Global Select Market
 
Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days.    Yes      No  

Indicate by check mark whether the registrant has submitted electronically every Interactive Data File required to be submitted pursuant to Rule 405 of Regulation S-T (§232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit such files).   Yes      No  

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, a smaller reporting company, or an emerging growth company. See the definitions of large"large accelerated filer, accelerated filer, smallerfiler", "accelerated filer", "smaller reporting company,company", and "emerging growth company" in Rule 12b-2 of the Exchange Act.





Large accelerated filerAccelerated filer
Non-accelerated filer
  
Smaller reporting company
Emerging growth company

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.
Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act).    Yes      No  
The number of shares of the registrant’s Common Stock, $0.01 par value, outstanding as of April 25, 2023May 3, 2024 was 81,904,442.

78,799,694.


Table of Contents
INTEGRA LIFESCIENCES HOLDINGS CORPORATION
INDEX

 
 Page
Number



Table of Contents
PART I. FINANCIAL INFORMATION

Item 1. Financial Statements

INTEGRA LIFESCIENCES HOLDINGS CORPORATION
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
AND COMPREHENSIVE INCOME
(UNAUDITED)
(Dollars in thousands, except per share amounts)
Three Months Ended March 31,Three Months Ended March 31,
20232022 20242023
Total revenue, netTotal revenue, net$380,846 $376,638 
Costs and expenses:Costs and expenses:
Costs and expenses:
Costs and expenses:
Cost of goods sold
Cost of goods sold
Cost of goods soldCost of goods sold147,975 142,569 
Research and developmentResearch and development26,724 24,085 
Selling, general and administrativeSelling, general and administrative166,657 159,926 
Intangible asset amortizationIntangible asset amortization3,108 3,894 
Total costs and expensesTotal costs and expenses344,464 330,474 
Operating incomeOperating income36,382 46,164 
Interest incomeInterest income4,107 1,377 
Interest expenseInterest expense(12,100)(11,655)
Other income, net1,389 3,429 
Income before income taxes29,778 39,315 
Provision for income taxes5,552 6,414 
Net income$24,226 $32,901 
Net income per share
Other (expense) income, net
Other (expense) income, net
Other (expense) income, net
(Loss) income before income taxes
(Benefit) provision for income taxes
Net (loss) income
Net (loss) income per share
Net (loss) income per share
Net (loss) income per share
Basic
Basic
BasicBasic$0.30 $0.39 
DilutedDiluted$0.29 $0.39 
Weighted average common shares outstanding (See Note 13):Weighted average common shares outstanding (See Note 13):
Weighted average common shares outstanding (See Note 13):
Weighted average common shares outstanding (See Note 13):
Basic
Basic
BasicBasic81,871 83,632 
DilutedDiluted82,323 84,276 
Comprehensive income (See Note 14)Comprehensive income (See Note 14)21,02857,031 

The accompanying unaudited notes are an integral part of these condensed consolidated financial statements.
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INTEGRA LIFESCIENCES HOLDINGS CORPORATION
CONDENSED CONSOLIDATED BALANCE SHEETS (UNAUDITED)
(Dollars in thousands, except per share amounts)
March 31, 2023December 31, 2022
March 31, 2024March 31, 2024December 31, 2023
ASSETSASSETS
Current assets:Current assets:
Current assets:
Current assets:
Cash and cash equivalentsCash and cash equivalents$307,367 $456,661 
Trade accounts receivable, net of allowances of $3,544 and $4,304253,995 263,465 
Cash and cash equivalents
Cash and cash equivalents
Short-term investments
Trade accounts receivable, net of allowances of $5,050 and $4,879
Inventories, netInventories, net351,275 324,583 
Prepaid expenses and other current assets116,845 116,789 
Prepaid Expenses
Other Current Assets
Total current assetsTotal current assets1,029,482 1,161,498 
Property, plant and equipment, netProperty, plant and equipment, net315,175 311,302 
Right of use asset - operating leasesRight of use asset - operating leases146,514 148,284 
Intangible assets, netIntangible assets, net1,108,759 1,126,609 
GoodwillGoodwill1,041,606 1,038,881 
Deferred tax assets, netDeferred tax assets, net44,680 45,994 
Other assetsOther assets56,183 57,190 
Total assetsTotal assets$3,742,399 $3,889,758 
LIABILITIES AND STOCKHOLDERS’ EQUITYLIABILITIES AND STOCKHOLDERS’ EQUITY
Current liabilities:Current liabilities:
Current liabilities:
Current liabilities:
Current portion of borrowings under senior credit facilityCurrent portion of borrowings under senior credit facility$— $38,125 
Current portion of borrowings under senior credit facility
Current portion of borrowings under senior credit facility
Current portion of lease liability - operating leases
Current portion of lease liability - operating leases
Current portion of lease liability - operating leasesCurrent portion of lease liability - operating leases14,792 14,624 
Accounts payable, tradeAccounts payable, trade112,785 102,100 
Contract liabilitiesContract liabilities7,743 7,253 
Accrued compensationAccrued compensation53,611 78,771 
Accrued expenses and other current liabilitiesAccrued expenses and other current liabilities93,362 80,033 
Total current liabilitiesTotal current liabilities282,293 320,906 
Long-term borrowings under senior credit facilityLong-term borrowings under senior credit facility769,143 733,149 
Long-term borrowings under securitization facilityLong-term borrowings under securitization facility102,500 104,700 
Long-term convertible securitiesLong-term convertible securities568,069 567,341 
Lease liability - operating leasesLease liability - operating leases156,910 157,420 
Deferred tax liabilitiesDeferred tax liabilities61,693 63,338 
Other liabilitiesOther liabilities126,853 138,501 
Total liabilitiesTotal liabilities2,067,461 2,085,355 
Stockholders’ equity:Stockholders’ equity:
Preferred stock; no par value; 15,000 authorized shares; none outstandingPreferred stock; no par value; 15,000 authorized shares; none outstanding— — 
Common stock; $0.01 par value; 240,000 authorized shares; 90,813 and 90,477 issued at March 31, 2023 and December 31, 2022, respectively908 905 
Preferred stock; no par value; 15,000 authorized shares; none outstanding
Preferred stock; no par value; 15,000 authorized shares; none outstanding
Common stock; $0.01 par value; 240,000 authorized shares; 91,484 and 90,920 issued at March 31, 2024 and December 31, 2023, respectively
Additional paid-in capitalAdditional paid-in capital1,245,297 1,276,977 
Treasury stock, at cost; 8,918 shares and 6,823 shares at March 31, 2023 and December 31, 2022, respectively(481,678)(362,862)
Treasury stock, at cost; 12,735 shares and 12,751 shares at March 31, 2024 and December 31, 2023, respectively
Accumulated other comprehensive lossAccumulated other comprehensive loss7,067 10,265 
Retained earningsRetained earnings903,344 879,118 
Total stockholders’ equityTotal stockholders’ equity1,674,938 1,804,403 
Total liabilities and stockholders’ equityTotal liabilities and stockholders’ equity$3,742,399 $3,889,758 
The accompanying unaudited notes are an integral part of these condensed consolidated financial statements.
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INTEGRA LIFESCIENCES HOLDINGS CORPORATION
CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS
(UNAUDITED)
(Dollars in thousands)
Three Months Ended March 31, Three Months Ended March 31,
20232022 20242023
OPERATING ACTIVITIES:OPERATING ACTIVITIES:
Net income$24,226 $32,901 
Net (Loss) Income
Net (Loss) Income
Net (Loss) Income
Adjustments to reconcile net income to net cash provided by operating activities:Adjustments to reconcile net income to net cash provided by operating activities:
Depreciation and amortizationDepreciation and amortization31,143 29,724 
Deferred income tax provision1,953 3,544 
Depreciation and amortization
Depreciation and amortization
Non-cash impairment charges
Deferred income tax provision (benefit)
Share-based compensationShare-based compensation3,620 6,291 
Amortization of debt issuance costs and expenses associated with debt refinancingAmortization of debt issuance costs and expenses associated with debt refinancing1,890 1,724 
Non-cash lease expenseNon-cash lease expense1,260 (17)
Loss (gain) on disposal of property and equipmentLoss (gain) on disposal of property and equipment(23)712 
Change in fair value of contingent consideration and others
Change in fair value of contingent consideration and others
Change in fair value of contingent consideration and othersChange in fair value of contingent consideration and others4,699 (765)
Changes in assets and liabilities:Changes in assets and liabilities:
Accounts receivable
Accounts receivable
Accounts receivableAccounts receivable10,041 (3,116)
InventoriesInventories(25,423)(11,561)
Prepaid expenses and other current assetsPrepaid expenses and other current assets(2,164)(5,046)
Other non-current assetsOther non-current assets(6,009)2,283 
Accounts payable, accrued expenses and other current liabilitiesAccounts payable, accrued expenses and other current liabilities(4,984)(9,754)
Contract liabilities
Other non-current liabilitiesOther non-current liabilities(14,073)(2,576)
Net cash provided by operating activitiesNet cash provided by operating activities26,156 44,344 
INVESTING ACTIVITIES:INVESTING ACTIVITIES:
Purchases of property and equipmentPurchases of property and equipment(13,704)(9,325)
Acquired in-process research and development milestone— (4,742)
Purchases of property and equipment
Purchases of property and equipment
Purchases of Investments
Purchases of Investments
Purchases of Investments
Net cash used in investing activities
Net cash used in investing activities
Net cash used in investing activitiesNet cash used in investing activities(13,704)(14,067)
FINANCING ACTIVITIES:FINANCING ACTIVITIES:
Proceeds from borrowings of long-term indebtedness
Proceeds from borrowings of long-term indebtedness
Proceeds from borrowings of long-term indebtednessProceeds from borrowings of long-term indebtedness10,200 11,250 
Payments on debtPayments on debt(12,400)(11,750)
Payment of debt issuance costsPayment of debt issuance costs(7,578)— 
Purchases of treasury stockPurchases of treasury stock(150,000)(125,000)
Proceeds from exercised stock optionsProceeds from exercised stock options2,326 1,239 
Cash taxes paid in net equity settlementCash taxes paid in net equity settlement(5,231)(9,204)
Net cash used in financing activities(162,683)(133,465)
Net cash provided by (used in) financing activities
Effect of exchange rate changes on cash and cash equivalentsEffect of exchange rate changes on cash and cash equivalents937 (3,168)
Net decrease in cash and cash equivalents(149,294)(106,356)
Net increase (decrease) in cash and cash equivalents
Cash and cash equivalents at beginning of periodCash and cash equivalents at beginning of period456,661 513,448 
Cash and cash equivalents at end of periodCash and cash equivalents at end of period$307,367 $407,092 
The accompanying unaudited notes are an integral part of these condensed consolidated financial statements.
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INTEGRA LIFESCIENCES HOLDINGS CORPORATION
CONDENSED CONSOLIDATED STATEMENTS OF CHANGES IN SHAREHOLDERS' EQUITY
(UNAUDITED)
(Dollars in thousands)
Three Months Ended March 31, 2023
Common StockTreasury StockAdditional Paid-In CapitalAccumulated Other Comprehensive LossRetained EarningsTotal Equity
SharesAmountSharesAmount
Balance, January 1, 202390,476 $905 (6,823)$(362,862)$1,276,977 $10,265 $879,118 $1,804,403 
Net income— — — — — — 24,226 24,226 
Three Months Ended March 31, 2024Three Months Ended March 31, 2024
Common StockCommon StockTreasury StockAdditional Paid-In CapitalAccumulated Other Comprehensive LossRetained EarningsTotal Equity
SharesAmountSharesAmount
Balance, January 1, 2024
Net loss
Other comprehensive income (loss), net of taxOther comprehensive income (loss), net of tax— — — — — (3,198)— (3,198)
Issuance of common stock through employee stock purchase planIssuance of common stock through employee stock purchase plan21 — — — 1,107 — — 1,107 
Issuance of common stock for vesting of share based awards, net of shares withheld for taxesIssuance of common stock for vesting of share based awards, net of shares withheld for taxes316 16 846 (4,858)— — (4,011)
Share-based compensationShare-based compensation— — — 3,609 — — 3,611 
Accelerated shares repurchasedAccelerated shares repurchased— $— (2,111)$(119,662)$(31,538)$— $— $(151,200)
Balance, March 31, 202390,813 $908 (8,918)$(481,678)$1,245,297 $7,067 $903,344 $1,674,938 
Balance, March 31, 2024
Three Months Ended March 31, 2022
Common StockTreasury StockAdditional Paid-In CapitalAccumulated Other Comprehensive LossRetained EarningsTotal Equity
SharesAmountSharesAmount
Balance, January 1, 202289,600 $896 (4,899)$(234,448)$1,264,943 $(45,155)$698,568 $1,684,804 
Three Months Ended March 31, 2023Three Months Ended March 31, 2023
Common StockCommon StockTreasury StockAdditional Paid-In CapitalAccumulated Other Comprehensive LossRetained EarningsTotal Equity
SharesAmountSharesAmount
Balance, January 1, 2023
Net incomeNet income— — — — — — 32,901 32,901 
Other comprehensive income (loss), net of taxOther comprehensive income (loss), net of tax— — — — — 24,130 — 24,130 
Issuance of common stock through employee stock purchase planIssuance of common stock through employee stock purchase plan17 — — — 1,078 — — 1,078 
Issuance of common stock for vesting of share based awards, net of shares withheld for taxesIssuance of common stock for vesting of share based awards, net of shares withheld for taxes339 14 714 (9,758)— — (9,040)
Share-based compensationShare-based compensation— — — — 6,324 — — 6,324 
Accelerated shares repurchasedAccelerated shares repurchased— — (1,938)(129,152)4,152 — — (125,000)
Balance, March 31, 202289,956 $900 (6,823)$(362,886)$1,266,739 $(21,025)$731,469 $1,615,197 
Balance, March 31, 2023
The accompanying unaudited notes are an integral part of these condensed consolidated financial statements.
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INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED)

1. BASIS OF PRESENTATION
General
The terms “we,” “our,” “us,” “Company” and “Integra” refer to Integra LifeSciences Holdings Corporation, a Delaware corporation, and its subsidiaries unless the context suggests otherwise.
In the opinion of management, the March 31, 20232024 unaudited condensed consolidated financial statements contain all adjustments (consisting only of normal recurring adjustments) necessary for a fair statement of the financial position, statement of changes in shareholders'shareholders’ equity, results of operations and cash flows of the Company. Certain information and footnote disclosures normally included in financial statements prepared in accordance with generally accepted accounting principles in the United States ("GAAP"(“GAAP”) have been condensed or omitted in accordance with the instructions to Form 10-Q and Rule 10-01 of Regulation S-X. These unaudited condensed consolidated financial statements should be read in conjunction with the Company’s consolidated financial statements for the year ended December 31, 20222023 included in the Company’s Annual Report on Form 10-K. The December 31, 20222023 consolidated balance sheet was derived from audited financial statements, but does not include all disclosures required by GAAP. Operating results for the three-month period ended March 31, 20232024 are not necessarily indicative of the results to be expected for the entire year.
The preparation of consolidated financial statements is in conformity with GAAP, which requires management to make estimates and assumptions that affect the reported amount of assets and liabilities, the disclosure of contingent liabilities, and the reported amounts of revenues and expenses. Significant estimates affecting amounts reported or disclosed in the condensed consolidated financial statements include allowances for doubtful accounts receivable and sales returns and allowances, net realizable value of inventories, valuation of intangible assets including amortization periods for acquired intangible assets, discount rates and estimated projected cash flows used to value and test impairments of long-lived assets and goodwill, estimates of projected cash flows and depreciation and amortization periods for long-lived assets, computation of taxes, valuation allowances recorded against deferred tax assets, the valuation of stock-based compensation, valuation of derivative instruments, valuation of contingent liabilities, the fair value of debt instruments and loss contingencies. These estimates are based on historical experience and on various other assumptions that are believed to be reasonable under the current circumstances. Actual results could differ from these estimates.

Recent Accounting Pronouncements
In March 2020, the FASBFinancial Accounting Standards Board (“FASB”) issued ASU 2020-04, Reference Rate Reform (Topic 848): Facilitation of the Effects of Reference Rate Reform on Financial Reporting(Topic 848), and, subsequent amendment toin January 2021, subsequently amended the initial guidance:guidance in: ASU 2021-01, Reference Rate Reform (Topic 848): Scope (collectively, “Topic 848”). Topic 848 provides optional expedients and exceptions for applying GAAP to contracts, hedging relationships, and other transactions affected by reference rate reform if certain criteria are met. The amendments apply only to contracts, hedging relationships, and other transactions that reference London Inter-Bank Offered Rate ("LIBOR"(“LIBOR”) or another reference rate expected to be discontinued because of reference rate reform. The guidance generally can be applied throughIn December 2022, the FASB issued ASU 2022-06, Reference Rate Reform (Topic 848): Deferral of the Sunset Date of Topic 848, which delayed the effective date from December 31, 2022 to December 31, 2024.The Alternative Reference Rates Committee, a group of private-market participants convened by the U.S. Federal Reserve Board and the New York Federal Reserve, has recommended the use of the Secured Overnight Financing Rate ("SOFR"(“SOFR”) as a more robust reference rate alternative to LIBOR. The use of SOFR as a substitute for LIBOR is, however, voluntary and may not be suitable for all market participants. There can be no assurance that the replacement rate will be economically equivalent to LIBOR, which could result in higher interest rates for us under our debt facilities. There is no guarantee that a transition from LIBOR to SOFR will not result in financial market disruptions, significant increases in benchmark rates, or our borrowing costs, any of which could have an adverse effect on our business, results of operations and financial condition. On March 24, 2023, the Company entered into the seventh amendment and restatement (the "March“March 2023 Amendment"Amendment”) of its Senior Credit Facility (the “Senior Credit Facility”) with a syndicate of lending banks with Bank of America, N.A., as Administrative Agent. In connection with the March 2023 Amendment, the Company replaced all LIBOR-based contracts with SOFR, which is calculated based on overnight transactions under repurchase agreements backed by Treasury securitiessecurities. In addition, on April 17, 2023 the Company entered into an amendment (the “April 2023 Amendment”) of the Securitization Facility (as defined below) and amended the interest rate from LIBOR to SOFR indexed rate. (See Note 6)6, Debt). In March 2023, the Company entered into a basis swap where the Company receives Term SOFR and pays LIBOR to convert the portfolio of interest rate swaps from LIBOR to SOFR. Integra has elected to adopt the optional expedient under ASCTopic 848, which will allow the interest rate swap hedging relationship to continue, without de-designation, due to the change in the indexed rate from LIBOR to SOFR.
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INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
In December 2023, the FASB issued ASU 2023-09, Income Taxes (Topic 740): Improvements to Income Tax Disclosures which enhances the transparency of income tax disclosures by expanding annual disclosure requirements related to the rate reconciliation and income taxes paid. The amendments are effective for fiscal years beginning after December 15, 2023, and for interim periods within fiscal years beginning after December 15, 2024. Early adoption is permitted. The amendments should be applied retrospectively to all prior periods presented in the financial statements. The Company does not plan to early adopt and is currently evaluating this ASU to determine its impact on the Company’s disclosures.
In November 2023, the FASB issued ASU 2023-07, Segment Reporting (Topic 280): Improvements to Reportable Segment Disclosures, which updates reportable segment disclosure requirements primarily through enhanced disclosures about significant segment expenses. The amendments are effective for fiscal years beginning after December 15, 2023, and for interim periods within fiscal years beginning after December 15, 2024. Early adoption is permitted. The amendments should be applied retrospectively to all prior periods presented in the financial statements. The Company does not plan to early adopt and is currently evaluating this ASU to determine its impact on the Company’s disclosures.
There are no other recently issued accounting pronouncements that are expected to have any significant effect on the Company'sCompany’s financial position, results of operations or cash flows.
8

INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
2. ACQUISITIONS AND DIVESTITURES
Surgical Innovation Associates,Acquisition of Acclarent Inc. Acquisition

OnIn December 6, 2022,2023, the Company completed its acquisitionentered into a definitive agreement to acquire Acclarent, Inc. (“Acclarent”) from Ethicon, Inc., a subsidiary of Surgical Innovation Associates, Inc. ("SIA")Johnson & Johnson, for an acquisition$275.0 million in cash at closing, subject to customary purchase price adjustments, and an additional $5.0 million contingent upon the achievement of $51.5 million (the "SIA Acquisition"). In additiona regulatory milestone, which was achieved prior to the purchase price, the acquisition includes two separate contingent considerations payments, which are dependent on 1) achieving certain revenue-based performance milestones in 2023, 2024, and 2025 (up to $50.0 million in additional payments), as well as 2) the approval by the FDA of the Premarket Approval (“PMA”) Application for DuraSorb for certain uses by certain timing targets (up to $40.0 million in additional payments). SIA's core technology, DuraSorb,closing. Acclarent is a fully resorbable scaffolddeveloper and marketer of a globally accepted polymer, which is cleared for usemedical devices used in hernia repair, abdominal wall, and other soft tissue reinforcement. DuraSorb salesEar, Nose, Throat (“ENT”) procedures. Acclarent’s results of operations will be reported within Integra’s Tissue Technologies ("TT")in the Company’s Codman Specialty Surgical reportable segment as partfrom the date of its Wound Reconstruction and Care franchise.acquisition.

Assets Acquired and Liabilities Assumed at Fair Value

The SIA Acquisition has been accounted for usingOn April 1, 2024, the Company successfully completed the acquisition method of accounting. This method requires that assets acquired, and liabilities assumed100% of Acclarent for approximately $282.0 million in a business combinationcash, subject to be recognized at their fair values ascustomary adjustments set forth in the purchase agreement related to working capital balances transferred to the Company. To facilitate the completion of the acquisition date.



The following table summarizesof Acclarent, the fair valuesCompany drew from the revolving portion of the assets acquired and liabilities assumed atSenior Credit Facility during the acquisition date:

Dollars in thousandsPreliminary ValuationWeighted Average Life
Current assets:
Cash4,438 
Trade accounts receivable, net1,551 
Inventories, net2,900 
Prepaid expenses and other current assets1,654 
Total current assets$10,543 
Intangible assets75,000 14 years
Goodwill41,854 
Total assets acquired$127,397
Current liabilities:
Accounts payable and accrued expenses$2,044 
Total current liabilities$2,044 
Deferred Tax Liability11,799 
Contingent consideration57,607 
Total liabilities assumed71,450
Net assets acquired$55,947

Developed Technology

The estimated fair value of the developed technology was determined using the multi-period excess earnings method of the income approach, which estimates value basedthree months ended March 31, 2024. For further detail on the present value of future economic benefits. Some of the more significant assumptions inherent in the development of those asset valuations include the estimated net cash flows for each year for each product including net revenues, cost of sales, R&D costs, selling and marketing costs, working capital, and contributory asset charges, the appropriate discount rate to select in order to measure the risk inherent in each future cash flow stream, the assessment of the asset’s life cycle, and competitive trends impacting the asset and the cash flow stream.

The Company used a discount rate of 18% to arrive at the present value for the acquired intangible assets to reflect the rate of return a market participant would expect to earn and incremental commercial uncertainty in the cash flow projections. No assurances can be given that the underlying assumptions used to prepare the discounted cash flow analysis will not change. For these and other reasons, actual results may vary significantly from estimated results.



9

INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
Goodwill

The Company allocated goodwill related to the SIA Acquisition to the TT segment. Goodwill is the excess of the consideration transferred over the net assets recognized and represents the expected revenue and cost synergies of the combined company and assembled workforce. A key factor that contributes to the recognition of goodwill, and a driver for the Company’s acquisition of SIA, is the attractive growth opportunities presented by the surgical matrix business in the breast reconstruction market. Goodwill recognized as a result of this acquisition is non-deductible for income tax purposes.

Contingent Consideration

The Company determines the acquisition date fair value of contingent consideration obligations based on a probability-weighted income approach derived from revenue estimates and a probability assessment with respect to the likelihood of achieving contingent obligations. The fair value measurement is based on significant inputs not observable in the market and thus represents a Level 3 measurement as defined using the fair value concepts in ASC 820. The resulting most likely payouts are discounted using an appropriate effective annual interest rate. At each reporting date, the contingent consideration obligation will be revalued to estimated fair value and changes in fair value will be reflected as income or expense in the consolidated statement of operations. Changes in the fair value of the contingent considerations may result from changes in discount periods and rates and changes in the timing and amount of revenue estimates. Changes in assumptions utilized in the contingent consideration fair value estimates could result in an increase in the contingent consideration obligation and a corresponding charge to operating results.

As part of the SIA Acquisition, the Company is required to pay to the shareholder of SIA up to $90.0 million for two separate payments, which are dependent on 1) achieving certain revenue-based performance milestones in 2023, 2024, and 2025 (up to $50.0 million in additional payments), as well as 2) the approval by the FDA of the PMA for DuraSorb for certain uses by certain timing targets (up to $40.0 million in additional payments). The Company used iterations of the Monte Carlo simulation to calculate the fair value of the contingent consideration for the revenue-based milestone that considered the possible outcomes of scenarios related to each specific milestone for the revenue based performance milestone. The Company used probabilities of achieving the conditions to calculate the fair value of the contingent consideration for the PMA approval milestone. The Company estimated the fair value of the contingent consideration for the revenue based milestone to be $32.6 million at the acquisition date and $25.0 million for the PMA approval milestone as of December 31, 2022. The company recorded a total of $48.7 million in other liabilities as of March 31, 2023 and $12.5 million in accrued expenses and other current liabilities at March 31, 2023 in the consolidated balance sheet of the company.borrowings, see The change in the fair value of the contingent obligation was primarily as a result of changes in the timing.Note 6. Debt

.
Deferred Tax Liabilities

Deferred tax liabilities result from identifiable intangible assets’ fair value adjustments. These adjustments create excess book basis over tax basis which is tax-effected by the statutory tax rates of applicable jurisdictions.

Sale of non-core traditional wound care business
On August 31, 2022, the Company completed its sale of its non-core traditional wound care ("TWC") business to Gentell, LLC ("Gentell") for $28.8 million, which consists of $27.8 million in cash plus $1.0 million in contingent consideration which may be received upon achieving certain revenue-based performance milestones two years after the closing date. The proceeds from the sale of the TWC business of $27.8 million is presented in the consolidated statement of cash flows net of cash transferred of $3.5 million and other transaction fees. The transaction included the sale of the Company's TWC products, such as sponges, gauze and conforming bandages, and certain advanced wound care dressings, such as supportive, calcium alginate, hydrogel, and foam dressings.
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INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
The divestiture did not represent a strategic shift that had a major effect on the Company's operations and financial statements. Goodwill was allocated to the assets and liabilities divested using the relative fair value method of the TWC business to the Company's TT reportable business segment. In connection with the sale, the Company recognized $0.6 million as a gain from the sale of the business in the condensed consolidated statement of operations for the year ended December 31, 2022. The transaction is subject to final working capital adjustments.
In addition to the purchase and sale agreement, the Company also entered into a contract manufacturing agreement with Gentell. Under the terms of the agreement, Gentell received inventory, equipment, and tooling to manufacture certain MediHoney® and TCC-EZ® products on behalf of the Company. On the close date of this transaction, the Company transferred all inventory associated with these products to Gentell and recognized an asset of $11.1 million, as a form of a deposit for the inventory transferred, which based on the expected timing of inventory purchases, was primarily included within prepaid expenses and other current assets in the consolidated balance sheet. This deposit will be utilized by the Company on future orders placed to Gentell for such products. As of March 31, 2023, the Company had a deposit remaining of $7.3 million which is included in prepaid assets and recognized a payable due to Gentell of $0.7 million, which is included in the condensed consolidated balance sheet within accrued expenses and other current liabilities.
3. REVENUES FROM CONTRACTS WITH CUSTOMERS
Summary of Accounting Policies on Revenue Recognition
Revenue is recognized upon the transfer of control of promised products or services to the customers in an amount that reflects the consideration the Company expects to receive in exchange for those products and services.
Performance Obligations
The Company'sCompany’s performance obligations consist mainly of transferring control of goods and services identified in the contracts, purchase orders, or invoices. The Company has no significant multi-element contracts with customers.
Significant Estimates
Usage-based royalties and licenses are estimated based on the provisions of contracts with customers and recognized in the same period that the royalty-based products are sold by the Company'sCompany’s strategic partners. The Company estimates and recognizes royalty revenue based upon communication with licensees, historical information, and expected sales trends. Differences between actual reported licensee sales and those that were estimated are adjusted in the period in which they become known, which is typically the following quarter. Historically, such adjustments have not been significant.
The Company estimates returns, price concessions, and discount allowances using the expected value method based on historical trends and other known factors. Rebate allowances are estimated using the most likely method based on each customer contract.
The Company'sCompany’s return policy, as set forth in its product catalogs and sales invoices, requires review and authorization in advance prior to the return of product. Upon the authorization, a credit will be issued for the goods returned within a set amount of days from the shipment, which is generally 90 days.
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INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
In 2023, due to the voluntary recall of all products manufactured at the Boston facility, including PriMatrix®, SurgiMend®, Revize™, and TissueMend™ (the “Boston recall”), the Company recorded a total of $18.7 million provision for product returns. As of March 31, 2024, the Company has credited $16.7 million to customers and holds a remaining return reserve of $2.0 million.
The Company disregards the effects of a financing component if the Company expects, at contract inception, that the period between the transfer and customer payment for the goods or services will be one year or less. The Company has no significant revenues recognized on payments expected to be received more than one year after the transfer of control of products or services to customers.
Contract Asset and Liability
Revenues recognized from the Company'sCompany’s private label business that are not invoiced to the customers as a result of recognizing revenue over time are recorded as a contract asset included in the prepaid expenses and other current assets account in the consolidated balance sheets.
Other operating revenues may include fees received under service agreements. Non-refundable fees received under multiple-period service agreements are recognized as revenue as the Company satisfies the performance obligations to the other party. A portion of the transaction price allocated to the performance obligations to be satisfied in the future periods is recognized as contract liability.
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INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
The following table summarizedsummarizes the changes in the contract asset and liability balances for the three months ended March 31, 2023:2024:
Dollars in thousandsTotal
Contract Asset
Contract asset, January 1, 20232024$10,1229,233 
Transferred to trade receivable from contract asset included in beginning of the year contract asset(9,765)(9,233)
Contract asset, net of transferred to trade receivables on contracts during the period9,7137,478 
Contract asset, March 31, 20232024$10,0707,478 
Contract Liability
Contract liability, January 1, 20232024$16,12716,252 
Recognition of revenue included in beginning of year contract liability$(3,523)(2,492)
Contract liability, net of revenue recognized on contracts during the period2,9212,017 
Foreign currency translation(63)
Contract liability, March 31, 20232024$16,55914,683 
At March 31, 2023,2024, the short-term portion of the contract liability of $7.7$7.8 million and the long-term portion of $8.8$6.9 million isare included in current liabilities and other liabilities, respectively, in the consolidated balance sheets.
As of March 31, 2023,2024, the Company is expected to recognize revenue of approximately 47%53% of unsatisfied (or partially unsatisfied) performance obligations as revenue within 12 months, with the remaining balance to be recognized thereafter.
Shipping and Handling Fees
The Company elected to account for shipping and handling activities as a fulfillment cost rather than a separate performance obligation. Amounts billed to customers for shipping and handling are included as part of the transaction price and recognized as revenue when control of underlying products is transferred to the customer. The related shipping and freight charges incurred by the Company are included in the cost of goods sold.
Product Warranties
Certain of the Company'sCompany’s medical devices, including monitoring systems and neurosurgical systems, are designed to operate over long periods of time. These products are sold with warranties which may extend for up to two years from the date of purchase. The warranties are not considered a separate performance obligation. The Company estimates its product warranties using the expected value method based on historical trends and other known factors. The Company includes them in accrued expenses and other current liabilities in the consolidated balance sheet.
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INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
Taxes Collected from Customers
The Company elected to exclude from the measurement of the transaction price all taxes assessed by a governmental authority that are both imposed on and concurrent with a specific revenue-producing transaction and collected by the entity from a customer.
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INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
Disaggregated Revenue
The following table presents revenues disaggregated by the major sources of revenues for the three months ended March 31, 20232024 and 20222023 (dollar amounts in thousands):
Three Months Ended March 31, 2023Three Months Ended March 31, 2022
Three Months Ended March 31, 2024
Three Months Ended March 31, 2024
Three Months Ended March 31, 2024Three Months Ended March 31, 2023
NeurosurgeryNeurosurgery$192,870 $194,675 
InstrumentsInstruments55,266 52,633 
Total Codman Specialty SurgicalTotal Codman Specialty Surgical248,136 247,308 
Wound Reconstruction and CareWound Reconstruction and Care100,940 94,630 
Wound Reconstruction and Care
Wound Reconstruction and Care
Private LabelPrivate Label31,770 34,700 
Total Tissue TechnologiesTotal Tissue Technologies132,710 129,330 
Total revenueTotal revenue$380,846 $376,638 
See Note 15, Segment and Geographical Information, for details of revenues based on the location of the customer.
4. INVENTORIES
Inventories, net consisted of the following:
Dollars in thousandsDollars in thousandsMarch 31, 2023December 31, 2022Dollars in thousandsMarch 31, 2024December 31, 2023
Finished goodsFinished goods$178,626 $172,088 
Work in processWork in process80,532 70,598 
Raw materialsRaw materials92,117 81,897 
Total inventories, netTotal inventories, net$351,275 $324,583 
5. GOODWILL AND OTHER INTANGIBLE ASSETS
Goodwill
Changes in the carrying amount of goodwill for the three-month period ended March 31, 20232024 were as follows:
Dollars in thousandsCodman Specialty
Surgical
Tissue TechnologiesTotal
Goodwill at December 31, 2022$656,219 $382,662 $1,038,881 
SIA Acquisition Working Capital Adjustment— 129 129 
Foreign currency translation1,639 957 2,596 
Goodwill at March 31, 2023$657,858 $383,748 $1,041,606 
Dollars in thousandsCodman Specialty
Surgical
Tissue TechnologiesTotal
Goodwill at December 31, 2023$666,937 $388,525 $1,055,462 
Foreign currency translation(9,622)(5,605)(15,227)
Goodwill at March 31, 2024$657,315 $382,920 $1,040,235 
The Company tests goodwill and intangible assets with indefinite lives for impairment annually in the third quarter in accordance with FASB ASC Topic 350, Intangibles—Goodwill and Other (“ASC 350”). Additionally, the Company may perform interim tests if an event occurs or circumstances change that could potentially reduce the fair value of a reporting unit or indefinite lived intangible asset below its carrying amount. The carrying value of each reporting unit is determined by assigning the assets and liabilities, including the existing goodwill and intangible assets, to those reporting units.
The Company tests for impairment by either performing a qualitative evaluation or a quantitative test. The qualitative evaluation is an assessment of factors, including reporting unit specific operating results as well as industry, market and general economic conditions, to determine whether it is more likely than not that the fair values of a reporting unit is less than its carrying amount, including goodwill. The Company may elect to bypass this qualitative evaluation for some or all of its reporting units and perform a quantitative test. The quantitative test estimates the fair value of the reporting unit using a
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NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
discounted cash flow model, which incorporates significant estimates and assumptions made by management which, by their nature, are characterized by uncertainty.
Due to third-party audit findings and an update to the estimated timeframe to resume the commercial distribution of products manufactured in the Boston facility, the Company elected to perform a quantitative analysis of its Tissue Technologies reporting unit in the first quarter of 2024 in accordance with ASC 350. The quantitative test estimates the fair value of the reporting unit using a discounted cash flow model, which incorporates significant estimates and assumptions made by management with respect to future revenue and expense growth rates and discount rates which, by their nature, are characterized by uncertainty. An impairment loss is recognized when the reporting unit’s carrying amount exceeds its estimated fair value. The quantitative test utilized a terminal growth rate of 2%, a discount rate of 15%, and a range and application of the company guideline multiples. The Company determined, after performing the quantitative analysis, that the fair value of the Tissue Technologies reporting unit was not less than its carrying amount, with 20% headroom.
Other Intangible Assets
The components of the Company’s identifiable intangible assets were as follows:
March 31, 2023 March 31, 2024
Dollars in thousandsDollars in thousandsWeighted
Average
Life
CostAccumulated
Amortization
NetDollars in thousandsWeighted
Average
Life
CostAccumulated
Amortization
Net
Completed technologyCompleted technology18 years$1,206,748 $(389,297)$817,451 
Customer relationshipsCustomer relationships12 years$193,297 $(146,098)$47,199 
Trademarks/brand namesTrademarks/brand names28 years$97,554 $(35,665)$61,889 
Codman tradenameCodman tradenameIndefinite$167,529 $— $167,529 
Supplier relationshipsSupplier relationships30 years$30,211 $(17,415)$12,796 
All otherAll other11 years$6,024 $(4,129)$1,895 
$1,701,363 $(592,604)$1,108,759 
$
December 31, 2022 December 31, 2023
Dollars in thousandsDollars in thousandsWeighted
Average
Life
CostAccumulated
Amortization
NetDollars in thousandsWeighted
Average
Life
CostAccumulated
Amortization
Net
Completed technologyCompleted technology18 years$1,204,325 $(370,968)$833,357 
Customer relationshipsCustomer relationships12 years193,081 (144,040)49,041 
Trademarks/brand namesTrademarks/brand names28 years97,265 (34,674)62,591 
Codman tradenameCodman tradenameIndefinite166,693 — 166,693 
Supplier relationshipsSupplier relationships30 years30,211 (17,170)13,041 
All otherAll other11 years5,957 (4,071)1,886 
$1,697,532 $(570,923)$1,126,609 
$
Total amortization of intangible assets for the three months ended March 31, 2024 was $27.7 million. Of these amounts, $17.6 million was related to amortization of technology based intangibles and included in cost of goods sold. $7.1 million related to the impairment of a customer relationship intangible and the remainder were included in intangible amortization in the statement of operations.
Total amortization of intangible assets for the three months ended March 31, 2023 was $20.6 million. Of these amounts, $17.5 million was related to amortization of technology based intangibles and included in cost of goods sold, with the remainder included in intangible amortization in the statement of operations.
Based on quarter-end exchange rates, amortization expense (including amounts reported in cost of goods sold) is expected to be approximately $61.8$60.1 million for the remainder of 2023, $81.8 million in 2024, $81.8$80.2 million in 2025, $81.6$80.0 million in 2026, $79.7$79.1 million in 2027, $78.1$78.7 million in 2028, $74.9 million in 2029 and $474.4$403.5 million thereafter.
The Company periodically performs testing for impairment on certain long-lived assets whenever events or changes in circumstances indicate that the carrying amount of an asset may not be recoverable.
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INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
Due to third-party audit findings and an update to the estimated timeframe to resume the commercial distribution of products manufactured in the Boston facility, the Company elected to perform impairment testing on certain definite-lived intangible assets including completed technology and customer relationships in accordance with FASB ASC Topic 360, Property, Plant and Equipment. For the three months ended March 31, 2024, the Company recorded an impairment charge related to the definite-lived intangible asset associated with the customer relationships of $7.1 million in intangible asset amortization in the consolidated statement of operations. With respect to the definite-lived intangible assets associated with the completed technology of SurgiMend® and PriMatrix®, the carrying values are $38.3 million and $27.7 million, respectively, as of March 31, 2024. We determined that the carrying amount of these definite-lived intangible assets were recoverable and, therefore, the intangible assets were not deemed to be impaired.
6. DEBT
Amendment to the Seventh Amended and Restated Senior Credit Agreement
On March 24, 2023, the Company entered into the Marchseventh amendment and restatement (the “March 2023 AmendmentAmendment”) of the Senior Credit Facility (the “Senior Credit Facility”) with a syndicate of lending banks with Bank of America, N.A., as Administrative Agent. The March 2023 Amendment extended the maturity date to March 24, 2028, amended the contractual repayments of Termthe term loan A,component, and amended the interest rate from LIBOR to SOFR-indexed interest. The Company continues to have the aggregate principal amount of up to approximately $2.1 billion available to it through the following facilities: (i) a $775.0 million term loan facility, and (ii) a $1.3 billion revolving credit facility, which includes a $60 million sublimit for the issuance of standby letters of credit and a $60 million sublimit for swingline loans.
The Company’s maximum consolidated total leverage ratio in the financial covenants (as defined in the Senior Credit Facility) was modified to the following:
Fiscal Quarter EndingMaximum Consolidated Total Leverage Ratio
March 31, 2023 through December 31, 20244.50 to 1.00
March 31, 2025 through June 30, 20264.25 to 1.00
September 30, 2026 and the last day of each fiscal quarter thereafter4.00 to 1.00
Borrowings under the Senior Credit Facility bear interest, at the Company’s option, at a rate equal to the following:
i.termTerm SOFR in effect from time to time plus 0.10% plus the applicable rate (ranging from 1.00% to 1.75%), or
ii.theThe highest of:
1.the weighted average overnight Federal funds rate, as published by the Federal Reserve Bank of New York, plus 0.50%;
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INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
2.the prime lending rate of Bank of America, N.A.; or
3.the one-month Term SOFR plus 1.00%.
The applicable rates are based on the Company’s consolidated total leverage ratio (defined as the ratio of (a) consolidated funded indebtedness as of such date less cash that is not subject to any restriction on the use or investment thereof to (b) consolidated EBITDA (as defined by the amended Seventh Amended and Restated Credit Agreement (the "Credit Agreement"“Credit Agreement”)), for the period of four consecutive fiscal quarters ending on such date).
The Company will pay an annual commitment fee (ranging from 0.15% to 0.30%), based on the Company'sCompany’s consolidated total leverage ratio, on the amount available for borrowing under the revolving credit facility.
The Senior Credit Facility is collateralized by substantially all of the assets of the Company’s U.S. subsidiaries, excluding intangible assets. The Senior Credit Facility is subject to various financial and negative covenants and, at March 31, 2023,2024, the Company was in compliance with all such covenants. The Company capitalized $7.6 million in deferred financing costs in connection with the modification of the Senior Credit Facility and wrote off $0.2 million of previously capitalized financing costs during the first quarter of 2023.
At March 31, 20232024 and December 31, 20222023 there was no balance$420.0 million and $70.0 million, respectively, outstanding under the revolving portion of the Senior Credit Facility. At March 31, 20232024 and December 31, 2022,2023, there was $775.0 million outstanding under the term loan component of the Senior Credit Facility at a weighted average interest rate of 6.3%6.8% and 5.6%6.8%, respectively. As of March 31, 2024 and December 31, 2023 there was no portion$19.4 million and $14.5 million, respectively, of the Term Loanterm loan component of the Senior Credit Facility classified as current on the condensed consolidated balance sheet. As of December 31, 2022, there was $38.1 million of the Term Loan component of the Senior Credit Facility classified as current on the consolidated balance sheets under the prior terms of the agreement.
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INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
The fair value of outstanding borrowings of the Senior Credit Facility's Term LoanFacility’s term loan component at March 31, 20232024 was $750.9$765.5 million. This fair value was determined by using a discounted cash flow model based on current market interest rates available to the Company. These inputs are corroborated by observable market data for similar liabilities and therefore classified within Level 2 of the fair value hierarchy. Level 2 inputs represent inputs that are observable for the asset or liability, either directly or indirectly, and are other than active market observable inputs that reflect unadjusted quoted prices for identical assets or liabilities.
Letters of credit outstanding as of March 31, 20232024 and December 31, 20222023 totaled $1.6$1.7 million. There were no amounts drawn under the letters of credit outstanding as of March 31, 2023.2024.
Contractual repayments of the Term Loanterm loan component of the Senior Credit Facility are due as follows:
Quarter Ended March 31, 2023Principal Repayment
As of March 31, 2024As of March 31, 2024Principal Repayment
Dollars in thousandsDollars in thousands
Remainder of 2023$— 
2024$14,531 
Remainder of 2024
Remainder of 2024
Remainder of 2024
20252025$33,906 
20262026$38,750 
2027
ThereafterThereafter687,813 
$775,000 
$
Future interest payments on the term loan component of the Senior Credit Facility based on current interest rates are expected to approximate $35.9$39.3 million for the remainder of 2023, $38.1 million in 2024, $32.6$50.8 million in 2025, $30.0$48.1 million in 2026, $45.0 million in 2027, and $34.5$10.0 million thereafter .thereafter. Interest is calculated on the term loan portion of the Senior Credit Facility based on SOFR plus the certain amounts set forth in the Credit Agreement. As the revolving credit facility and Securitization Facility (defined below) can be repaid at any time, no interest has been included in the calculation.
Any outstanding borrowings on the revolving credit component of the Senior Credit Facility isare due on March 24, 2028.
Convertible Senior Notes
On February 4, 2020, the Company issued $575.0 million aggregate principal amount of its 0.5% Convertible Senior Notes due 2025 (the "2025 Notes"“2025 Notes”). The 2025 Notes will mature on August 15, 2025 and bear interest at a rate of 0.5% per annum payable semi-annually in arrears, unless earlier converted, repurchased or redeemed in accordance with the terms of the 2025 Notes. In connection with this offering, the Company capitalized $13.2 million of financing fees.
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INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
The 2025 Notes are senior, unsecured obligations of the Company, and are convertible into cash and shares of its common stock based on an initial conversion rate, subject to adjustment of 13.5739 shares per $1,000 principal amounts of the 2025 Notes (which represents an initial conversion price of $73.67 per share). The 2025 Notes convert only in the following circumstances: (1) if the closing price of the Company'sCompany’s common stock has been at least 130% of the conversion price during the period; (2) if the average trading price per $1,000 principal amount of the 2025 Notes is less than or equal to 98% of the average conversion value of the 2025 Notes during a period as defined in the indenture; (3) at any time on or after February 20, 2023;if the Company calls the notes for optional redemption as defined in the indenture; or (4) if specified corporate transactions occur. As of March 31, 2023,2024, none of these conditions existed with respect to the 2025 Notes and as a result the 2025 Notes are classified as long term.term obligations.
On December 9, 2020, the Company entered into the First Supplemental Indenture to the original agreementindenture dated as of February 4, 2020 (the “Indenture”) between the Company and Citibank, N.A., as trustee, governing the Company’s outstanding 2025 Notes. The Company irrevocably elected (1) to eliminate the Company’s option to choose physical settlement on any conversion of the 2025 Notes that occurs on or after the date of the First Supplemental Indenture and (2) with respect to any Combination Settlement (as defined in the indenture) for a conversion of the 2025 Notes, the Specified Dollar Amount (as defined in the indenture) that will be settled in cash per $1,000 principal amount of the 2025 Notes shall be no lower than $1,000.
Holders of the 2025 Notes will have the right to require the Company to repurchase for cash all or a portion of their 2025 Notes at 100% of their principal amount, plus any accrued and unpaid interest, upon the occurrence of a fundamental change (as defined in the indenture relating to the 2025 Notes). The Company will also be required to increase the conversion rate for holders who convert their 2025 Notes in connection with certain fundamental changes occurring prior to the maturity date or following delivery by the Company of a notice of redemption.
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INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
In connection with the issuance of the 2025 Notes, the Company entered into call transactions and warrant transactions, primarily with affiliates of the initial purchasers of the 2025 Notes (the “hedge participants”). The cost of the call transactions was $104.2 million for the 2025 Notes. The Company received $44.5 million of proceeds from the warrant transactions for the 2025 Notes. The call transactions involved purchasing call options from the hedge participants, and the warrant transactions involved selling call options to the hedge participants with a higher strike price than the purchased call options. The initial strike price of the call transactions was $73.67, subject to anti-dilution adjustments substantially similar to those in the 2025 Notes. The initial strike price of the warrant transactions was $113.34 for the 2025 Notes, subject to customary anti-dilution adjustments.
At March 31, 20232024, the carrying amount of the liability was $575.0 million. The fair value of the 2025 Notes at March 31, 20232024 was $561.7549.7 million. Factors that the Company considered when estimating the fair value of the 2025 Notes included recent quoted market prices or dealer quote.quotes. The level of the 2025 Notes is considered asare valued based on Level 1.1 measurements in the fair value hierarchy.
Securitization Facility
In 2018, the Company entered into an accounts receivable securitization facility (the "Securitization Facility"“Securitization Facility”) under which accounts receivable of certain domestic subsidiaries are sold on a non-recourse basis to a special purpose entity (“SPE”), which is a bankruptcy-remote, consolidated subsidiary of the Company. Accordingly, the assets of the SPE are not available to satisfy the obligations of the Company or any of its subsidiaries. From time to time, the SPE may finance such accounts receivable with a revolving loan facility secured by a pledge of such accounts receivable. The amount of outstanding borrowings on the Securitization Facility at any one time is limited to $150.0 million. The Securitization Facility Agreement ("(“Securitization Agreement"Agreement”) governing the Securitization Facility contains certain covenants and termination events. An occurrence of an event of default or a termination event under this Securitization Agreement may give rise to the right of its counterparty to terminate this facility. As of March 31, 2023,2024, the Company was in compliance with the covenants and none of the termination events had occurred.
On May 28, 2021,December 15, 2023, the Company entered into an amendment (the "May 2021 Amendment"“December 2023 Amendment”) of the Securitization Facility which extended the maturity date from December 21, 2021 to May 28, 2024.2024 to December 15, 2026. The May 2021Company incurred approximately $0.3 million of new issuance costs associated with the December Amendment doeswhich will be amortized over 3 years, the length of the Securitization Agreement as amended by the December 2023 Amendment. Due to the increase in borrowing capacity, the remaining $0.1 million of unamortized costs from the previous agreement will also be amortized over the length of the amended agreement, 3 years. In addition, on April 17, 2023 the Company entered into an amendment (the “April 2023 Amendment”) of the Securitization Facility and amended the interest rate from LIBOR to SOFR-indexed rate. The December 2023 Amendment and April 2023 Amendment did not increase the Company’s total indebtedness.
The Securitization Facility is currently indexed to LIBOR. At March 31, 20232024 and December 31, 2022,2023, the Company had $102.5$94.6 million and $104.7$89.2 million, respectively, of outstanding borrowings under its Securitization Facility at a weighted average interest rate of 5.8%6.5% and 5.0%5.9%, respectively. In April 2023, we amended the facility to replace LIBOR with SOFR-indexed interest. The fair value of the outstanding borrowing of the Securitization Facility at March 31, 20232024 was $102.2$92.7 million. These fair values were determined by using a discounted cash flow model based on current market interest rates available to the Company. These inputs are corroborated by observable market data for similar liabilities and therefore classified within Level 2 of the fair value hierarchy. Level 2 inputs represent inputs that are observable for the asset or liability, either directly or indirectly, and are other than active market observable inputs that reflect unadjusted quoted prices for identical assets or liabilities.
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NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
7. DERIVATIVE INSTRUMENTS
Interest Rate Hedging
The Company’s interest rate risk relates to U.S. dollar denominated variable interest rate borrowings. The Company uses interest rate swap derivative instruments to manage earnings and cash flow exposure resulting from changes in interest rates. These interest rate swaps apply a fixed interest rate on a portion of the Company'sCompany’s expected SOFR-indexed borrowings. In connection with the March 2023 Amendment to the Senior Credit Facility, the Company amended its interest rate from LIBOR to SOFR-indexed interest. In March 2023, the Company entered into a basis swap where the Company receives Term SOFR and pays LIBORdaily compounded SOFR to convert the portfolio of swaps from LIBORdaily compounded SOFR to term SOFR.
The Company held the following interest rate swaps as of March 31, 20232024 and December 31, 20222023 (dollar amounts in thousands):
March 31, 2023March 31, 2023
March 31, 2024
March 31, 2024
March 31, 2024December 31, 2023March 31, 2024December 31, 2023
Hedged ItemHedged ItemNotional AmountDesignation DateEffective DateTermination DateFixed Interest RateEstimated Fair ValueHedged ItemNotional AmountDesignation DateEffective DateTermination DateFixed Interest RateEstimated Fair Value
Asset (Liability)
Asset (Liability)Asset (Liability)
1-month Term SOFR Loan1-month Term SOFR Loan150,000 December 13, 2017July 1, 2019June 30, 20242.423 %4,022 
1-month Term SOFR Loan1-month Term SOFR Loan200,000 December 13, 2017January 1, 2018December 31, 20242.313 %6,738 
1-month Term SOFR Loan1-month Term SOFR Loan75,000 October 10, 2018July 1, 2020June 30, 20253.220 %1,329 
1-month Term SOFR Loan1-month Term SOFR Loan75,000 October 10, 2018July 1, 2020June 30, 20253.199 %1,539 
1-month Term SOFR Loan1-month Term SOFR Loan75,000 October 10, 2018July 1, 2020June 30, 20253.209 %1,441 
1-month Term SOFR Loan1-month Term SOFR Loan100,000 December 18, 2018December 30, 2022December 31, 20272.885 %2,770 
1-month Term SOFR Loan1-month Term SOFR Loan100,000 December 18, 2018December 30, 2022December 31, 20272.867 %2,708 
1-month Term SOFR Loan1-month Term SOFR Loan575,000 December 15, 2020July 31, 2025December 31, 20271.415 %19,406 
1-month Term SOFR Loan1-month Term SOFR Loan125,000 December 15, 2020July 1, 2025December 31, 20271.404 %4,567 
Basis Swap (1)
Basis Swap (1)
March 31, 2023March 24, 2023December 31, 2027N/A(1,842)
$1,475,000 $42,678 
$
(1) The notional of the basis swap amortizes to match the total notional of the interest rate swap portfolio over time
(1) The notional of the basis swap amortizes to match the total notional of the interest rate swap portfolio over time

The interest rate swaps were carried on the consolidated balance sheet at fair value and changes in the fair values were recorded as unrealized gains or losses in accumulated other comprehensive income (“AOCI”). For the three months ended March 31, 2024 and 2023, the Company recorded a gain of $14.7 million and a loss of $10.5 million, respectively, in AOCI related to the change in fair value of the interest rate swaps.
17

INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
December 31, 2022December 31, 2022
Hedged ItemNotional AmountDesignation DateEffective DateTermination DateFixed Interest RateEstimated Fair Value
Asset (Liability)
1-month USD LIBOR Loan150,000 December 13, 2017July 1, 2019June 30, 20242.423 %5,012 
1-month USD LIBOR Loan200,000 December 13, 2017January 1, 2018December 31, 20242.313 %8,380 
1-month USD LIBOR Loan75,000 October 10, 2018July 1, 2020June 30, 20253.220 %1,831 
1-month USD LIBOR Loan75,000 October 10, 2018July 1, 2020June 30, 20253.199 %1,905 
1-month USD LIBOR Loan75,000 October 10, 2018July 1, 2020June 30, 20253.209 %1,970 
1-month USD LIBOR Loan100,000 December 18, 2018December 30, 2022December 31, 20272.885 %4,252 
1-month USD LIBOR Loan100,000 December 18, 2018December 30, 2022December 31, 20272.867 %4,153 
1-month USD LIBOR Loan575,000 December 15, 2020July 31, 2025December 31, 20271.415 %23,742 
1-month USD LIBOR Loan125,000 December 15, 2020July 1, 2025December 31, 20271.404 %5,467 
$1,475,000 $56,712 
For the three months ended March 31, 2024 and 2023, the Company recorded gains of $5.2 million and $3.5 million, respectively, in the consolidated statements of operations related to the interest rate differential of the interest rate swaps. The estimated gain that is expected to be reclassified to interest income from AOCI as of March 31, 2024 within the next twelve months is $13.6 million.
The Company has designated these derivative instruments as cash flow hedges. The Company assesses the effectiveness of these derivative instruments and has recorded the changes in the fair value of the derivative instrument designated as a cash flow hedge as unrealized gains or losses in accumulated other comprehensive loss (“AOCL”),AOCI, net of tax, until the hedged item affected earnings, at which point any gain or loss was reclassified to earnings. If the hedged cash flow does not occur, or if it becomes probable that it will not occur, the Company will reclassify the remaining amount of any gain or loss on the related cash flow hedge recorded in AOCLAOCI to interest expense at that time.
15

INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
Foreign Currency Hedging
From time to time, the Company enters into foreign currency hedge contracts intended to protect the U.S. dollar value of certain forecasted foreign currency denominated transactions. The Company assesses the effectiveness of the contracts that are designated as hedging instruments. The changes in fair value of foreign currency cash flow hedges are recorded in AOCL,AOCI, net of tax. Those amounts are subsequently reclassified to earnings from AOCLAOCI as impacted by the hedged item when the hedged item affects earnings. If the hedged forecasted transaction does not occur or if it becomes probable that it will not occur, the Company will reclassify the amount of any gain or loss on the related cash flow hedge to earnings at that time. For contracts not designated as hedging instruments, the changes in fair value of the contracts are recognized in other income, net in the consolidated statements of operation, along with the offsetting foreign currency gain or loss on the underlying assets or liabilities.
The success of the Company’s hedging anticipated currency exchange gains or losses to the extent that there are differences between forecasted and actual activities during periods of currency volatility. In addition, changes in currency exchange rates related to any unhedged transactions may affect earnings and cash flows.
Cross-Currency Rate Swaps
The objective of these cross-currency swaps is to reduce volatility of earnings and cash flows associated with changes in the foreign currency exchange rate. Under the terms of these contracts, which have been designated as cash flow hedges, the Company will make interest payments in Swiss francs (“CHFs”) and receive interest in U.S. dollars. Upon the maturity of these contracts, the Company will pay the principal amount of the loans in CHFs and receive U.S. dollars from the counterparties.
On September 26, 2022,22, 2023, the Company amended the CHF-denominatedSwiss franc denominated intercompany loan to partially settle CHF 20.0 million and extend the termination date to September 20232024 and as a result, the Company early terminated the cross-currency swap designated as cash flow hedge of an intercompany loan with aggregate notional amount of 50.0$48.5 million. Simultaneously, the Company entered into a cross-currency swap agreement to converthedge a notional amount of CHF 48.528.5 million equivalent to 49.1$31.5 million of this amended intercompany loan into U.S. dollars. The loss recorded by the Company upon the settlement of the swap was not material for the period.
On December 21, 2020, the Company entered into cross-currency swap agreements to convert a notional amount of $471.6 million equivalent to 420.1 million of a CHF-denominated intercompany loan into U.S. dollars. The CHF-denominated intercompany loan was the result of an intra-entity transfer of certain intellectual property rights to a subsidiary in Switzerland completed during the fourth quarter of 2020. The intercompany loan requires quarterly payments of CHF 5.8 million plus accrued interest. As a result, the aggregate notional amount of the related cross-currency swaps will decrease by a corresponding amount.
The Company held the following cross-currency rate swaps as of March 31, 2024 and December 31, 2023 (dollar amounts in thousands):
March 31, 2024December 31, 2023March 31, 2024December 31, 2023
Effective DateTermination DateFixed RateAggregate Notional AmountFair Value
Asset (Liability)
Pay CHFDecember 21, 2020December 22, 20253.00%CHF333,887 351,137 (9,902)(38,324)
Receive U.S.$3.98%$374,817 394,183 
Pay CHFSeptember 22, 2023September 29, 20242.40%CHF28,500 28,500 (2,578)(2,348)
Receive U.S.$6.27%$31,457 31,457 
Total$(12,480)$(40,672)
18
16

INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
The objective of these cross-currency swaps is to reduce volatility of earnings and cash flows associated with changes in the foreign currency exchange rate. Under the terms of these contracts, which have been designated as cash flow hedges, the Company will make interest payments in Swiss Francs and receive interest in U.S. dollars. Upon the maturity of these contracts, the Company will pay the principal amount of the loans in Swiss Francs and receive U.S. dollars from the counterparties.
The Company held the following cross-currency rate swaps as of March 31, 2023 and December 31, 2022 (dollar amounts in thousands):
March 31, 2023December 31, 2022March 31, 2023December 31, 2022
Effective DateTermination DateFixed RateAggregate Notional AmountFair Value
Asset (Liability)
Pay CHFDecember 21, 2020December 22, 20253.00%CHF373,227 397,137 (3,033)(4,241)
Receive U.S.$3.98%$418,980 445,821 
Pay CHFSeptember 28, 2022September 29, 20231.95%CHF48,533 48,532 (4,011)(3,528)
Receive U.S.$5.32%$49,142 49,142 
Total$(7,044)$(7,769)
The cross-currency swaps are carried on the consolidated balance sheet at fair value, and changes in the fair values are recorded as unrealized gains or losses in AOCL.AOCI. For the three months ended March 31, 2024 the Company recorded a gain of $30.1 million in other income, net related to change in fair value related to the foreign currency rate translation to offset the losses recognized on the intercompany loans. For the three months ended March 31, 2023, and 2022, the Company recorded a loss of $4.9 million and a gain $6.5 million, respectively, in other income, net related to change in fair value related to the foreign currency rate translation to offset the losses recognized on the intercompany loans.
For the three months ended March 31, 2023, and 2022,2024, the Company recorded a gain of $7.5 million and $7.9$29.5 million in AOCL, respectively,AOCI related to change in fair value of the cross-currency swaps. For the three months ended March 31, 2023, the Company recorded a gain of $2.2 million in AOCI related to change in fair value of the cross-currency swaps.
For the three months ended March 31, 2024, the Company recorded a gain of $1.3 million in other income, net included in the consolidated statements of operations related to the interest rate differential of the cross-currency swaps. For the three months ended March 31, 2023, and 2022, the Company recorded a gain of $1.5 million and $1.8 million, respectively, in other income, net included in the consolidated statements of operations related to the interest rate differential of the cross-currency swaps.
The estimated gainloss that is expected to be reclassified to other income (expense), net from AOCLAOCI as of March 31, 20232024 within the next twelve months is $0.1$1.9 million. As of March 31, 2023,2024, the Company does not expect any gains or losses will be reclassified into earnings as a result of the discontinuance of these cash flow hedges because the original forecasted transactiontransactions will not occur.
Net Investment Hedges
The Company manages certain foreign exchange risks through a variety of strategies, including hedging. The Company is exposed to foreign exchange risk from its international operations through foreign currency purchases, net investments in foreign subsidiaries, and foreign currency assets and liabilities created in the normal course of business. On October 1, 2018 May 24, 2022, and December 16, 2020,November 17, 2023, the Company entered into cross-currency swap agreements designated as net investment hedges to partially offset the effects of foreign currency on foreign subsidiaries.
19

INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
The Company held the following cross-currency rate swaps designated as net investment hedges as of March 31, 20232024 and December 31, 2022,2023, respectively (dollar amounts in thousands):
March 31, 2024March 31, 2024December 31, 2023March 31, 2024December 31, 2023
Effective DateEffective DateTermination DateFixed RateAggregate Notional AmountFair Value
Asset (Liability)
March 31, 2023December 31, 2022March 31, 2023December 31, 2022
Effective DateTermination DateFixed RateAggregate Notional AmountFair Value
Asset (Liability)
Pay EUR
Pay EUR
Pay EURPay EUROctober 3, 2018September 30, 2023—%EUR51,760 51,760 3,989 4,713 
Receive U.S.$Receive U.S.$2.57%$60,000 60,000 
Pay EUROctober 3, 2018September 30, 2025—%EUR38,820 38,820 3,932 4,307 
Pay CHF
Pay CHF
Pay CHF
Receive U.S.$Receive U.S.$October 3, 2018September 30, 20252.19%$45,000 45,000 3,932 4,307 
Pay CHF
Pay CHF
Pay CHFPay CHFMay 26, 2022December 16, 2028—%CHF288,210 288,210 (14,711)(14,663)
Receive U.S.$Receive U.S.$1.94%$300,000 300,000 
TotalTotal$(6,790)$(5,643)
Total
Total
The cross-currency swaps were carried on the consolidated balance sheet at fair value and changes in the fair values were recorded as unrealized gains or losses in AOCL.AOCI. For the three months ended March 31, 2024, the Company recorded a gain of $24.9 million in AOCI related to the change in fair value of the cross-currency swaps. For the three months ended March 31, 2023, and 2022, the Company recorded a lossgain of $1.1$1.0 million and a gain $1.3 million, respectively, in AOCLAOCI related to the change in fair value of the cross-currency swaps.
For the three months ended March 31, 2023, and 2022,2024, the Company recorded gainsa gain of $2.2 million in interest income included in the consolidated statements of operations related to the interest rate differential of the cross-currency swaps. For the three months ended March 31, 2023, the Company recorded a gain of $2.1 million and $1.3 million, respectively, in interest income included in the consolidated statements of operations related to the interest rate differential of the cross-currency swaps.
The estimated gain that is expected to be reclassified to interest income from AOCLAOCI as of March 31, 20232024 within the next twelve months is $10.9$4.1 million.
17

INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
On May 2, 2024, the Company entered into a cross-currency swap agreement with a notional amount of CHF 68.5 million, equivalent to $75.0 million, where the Company agreed with third-parties to sell Swiss francs in exchange for U.S. dollars at a specified rate at the maturity of the contract. The new cross-currency swap agreement was designated as a net investment hedge to partially offset the effects of foreign currency on foreign subsidiaries.
Foreign Currency Forward ContractContracts
The Company has entered into a hedge for forecasted intercompany purchases denominated in foreign currencies through the use of forward contracts designated as cash flow hedges. To the extent these forward contracts meet hedge accounting criteria, changes in their fair value are not included in accumulated comprehensive loss. These changes in fair value will be recognized into earnings as a component of cost of sales when the forecasted-transaction occurs.
DuringIn the first quarter of 20232024, the Company entered into Foreign Currency Forward Contracts with aforeign currency forwards to mitigate the exchange rate risk of Swiss franc denominated intercompany purchases. These contracts typically settle at various dates within twelve months of execution. As of March 31, 2024 the notional amount of $10.8 million to mitigate the risk of foreign currency on intercompany purchases in CHF. Duringforward contracts was CHF13.3 million. For the three months ended March 31, 20232024 the Company recorded an immateriala loss of $0.6 million in AOCLAOCI related to the change in fair value of the Foreign Currency Forward Contracts.foreign currency forward contracts and a loss of $0.1 million in cost of goods sold included in the consolidated statements of operations.
Counterparty Credit Risk
The Company manages its concentration of counterparty credit risk on its derivative instruments by limiting acceptable counterparties to a group of major financial institutions with investment grade credit ratings, and by actively monitoring their credit ratings and outstanding positions on an ongoing basis. Therefore, the Company considers the credit risk of the counterparties to be low. Furthermore, none of the Company’s derivative transactions are subject to collateral or other security arrangements, and none contain provisions that depend upon the Company’s credit ratings from any credit rating agency.
Fair Value of Derivative Instruments
The Company has classified all of its derivative instruments within Level 2 of the fair value hierarchy because observable inputs are available for substantially the full term of the derivative instruments. The fair values of the interest rate swaps and cross-currency swaps were developed using a market approach based on publicly available market yield curves and the terms of the swap. The Company performs ongoing assessments of counterparty credit risk.
2018

INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
The following table summarizes the fair value for derivatives designated as hedging instruments in the condensed consolidated balance sheets as of March 31, 20232024 and December 31, 2022:2023:
Fair Value as of
Fair Value as of
Fair Value as of
Fair Value as of
Location on Balance Sheet (1):
Location on Balance Sheet (1):
Location on Balance Sheet (1):
Location on Balance Sheet (1):
March 31, 2023December 31, 2022
Dollars in thousandsDollars in thousands
Dollars in thousands
Dollars in thousands
Derivatives designated as hedges — Assets:
Derivatives designated as hedges — Assets:
Derivatives designated as hedges — Assets:Derivatives designated as hedges — Assets:
Prepaid expenses and other current assetsPrepaid expenses and other current assets
Prepaid expenses and other current assets
Prepaid expenses and other current assets
Cash Flow Hedges
Cash Flow Hedges
Cash Flow HedgesCash Flow Hedges
Interest rate swap(2)
Interest rate swap(2)
$15,659 $16,682 
Interest rate swap(2)
Interest rate swap(2)
Cross-currency swap
Cross-currency swap
Cross-currency swapCross-currency swap4,139 4,497 
Net Investment HedgesNet Investment Hedges
Net Investment Hedges
Net Investment Hedges
Cross-currency swap
Cross-currency swap
Cross-currency swapCross-currency swap10,942 11,653 
Other assetsOther assets
Other assets
Other assets
Cash Flow Hedges
Cash Flow Hedges
Cash Flow HedgesCash Flow Hedges
Interest rate swap(2)
Interest rate swap(2)
28,861 40,030 
Interest rate swap(2)
Interest rate swap(2)
Cross-currency swap
Cross-currency swap
Cross-currency swapCross-currency swap— — 
Net Investment HedgesNet Investment Hedges
Net Investment Hedges
Net Investment Hedges
Cross-currency swapCross-currency swap2,940 3,311 
Cross-currency swap
Cross-currency swap
Total derivatives designated as hedges — Assets
Total derivatives designated as hedges — Assets
Total derivatives designated as hedges — AssetsTotal derivatives designated as hedges — Assets$62,541 $76,173 
Derivatives designated as hedges — Liabilities:Derivatives designated as hedges — Liabilities:
Derivatives designated as hedges — Liabilities:
Derivatives designated as hedges — Liabilities:
Accrued expenses and other current liabilities
Accrued expenses and other current liabilities
Accrued expenses and other current liabilitiesAccrued expenses and other current liabilities
Cash Flow HedgesCash Flow Hedges
Cash Flow Hedges
Cash Flow Hedges
Interest rate swap(2)
Interest rate swap(2)
Interest rate swap(2)
Interest rate swap(2)
$762 $— 
Cross-currency swapCross-currency swap4,011 3,528 
Cross-currency swap
Cross-currency swap
Foreign currency forward contracts
Foreign currency forward contracts
Foreign currency forward contractsForeign currency forward contracts69 
Net Investment HedgesNet Investment Hedges
Net Investment Hedges
Net Investment Hedges
Cross-currency swap
Cross-currency swap
Cross-currency swapCross-currency swap— — 
Other liabilitiesOther liabilities
Other liabilities
Other liabilities
Cash Flow Hedges
Cash Flow Hedges
Cash Flow HedgesCash Flow Hedges
Interest rate swap(2)
Interest rate swap(2)
1,080 — 
Interest rate swap(2)
Interest rate swap(2)
Cross-currency swap
Cross-currency swap
Cross-currency swapCross-currency swap7,172 8,738 
Net Investment HedgesNet Investment Hedges
Net Investment Hedges
Net Investment Hedges
Cross-currency swap
Cross-currency swap
Cross-currency swapCross-currency swap20,672 20,608 
Total derivatives designated as hedges — LiabilitiesTotal derivatives designated as hedges — Liabilities$33,766 $32,874 
Total derivatives designated as hedges — Liabilities
Total derivatives designated as hedges — Liabilities
(1) The Company classifies derivative assets and liabilities as current based on the cash flows expected to be incurred within the following 12 months.
(2) At March 31, 20232024 and December 31, 2022,2023, the total notional amounts related to the Company’s interest rate swaps were both $1.5 billion, respectively.billion.
2119

INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
The following presents the effect of derivative instruments designated as cash flow hedges and net investment hedges on the accompanying condensed consolidated statement of operations during the three months ended March 31, 20232024 and 2022:2023:
Dollars in thousandsDollars in thousandsBalance in AOCL
Beginning of
Quarter
Amount of
Gain (Loss)
Recognized in
AOCL
Amount of Gain (Loss)
Reclassified from
AOCL into
Earnings
Balance in AOCL
End of Quarter
Location in
Statements of
Operations
Dollars in thousandsBalance in AOCI
Beginning of
Quarter
Amount of
Gain (Loss)
Recognized in
AOCI
Amount of Gain (Loss)
Reclassified from
AOCI into
Earnings
Balance in AOCI
End of Quarter
Location in
Statements of
Operations
Three Months Ended March 31, 2023
Cash Flow Hedges
Interest rate swap$56,712 $(10,534)$3,500 $42,678 Interest expense
Cross-currency swap(20,271)2,191 (3,504)(14,576)Other income, net
Foreign Currency Forward Contract— (69)— (69)Cost of Sales
Net Investment Hedges
Cross-currency swap(6,914)950 2,096 (8,060)Interest income
$29,527 $(7,462)$2,092 $19,973 
Three Months Ended March 31, 2022
Cash Flow Hedges
Interest rate swap$(43,956)$41,675 $(5,213)$2,932 Interest expense
Cross-currency swap(9,688)316 8,331 (17,703)Other income, net
Net Investment Hedges
Cross-currency swap(2,312)1,309 1,320 (2,323)Interest income
$(55,956)$43,300 $4,438 $(17,094)
Three Months Ended March 31, 2024
Three Months Ended March 31, 2024
Three Months Ended March 31, 2024
Cash Flow Hedges
Cash Flow Hedges
Cash Flow Hedges
Interest rate swap
Interest rate swap
Interest rate swap$43,556 $14,723 $5,219 $53,060 Interest expense
Cross-currency swapCross-currency swap(15,763)29,532 31,473 (17,704)Other income (expense), net
Foreign currency forward contractForeign currency forward contract— (629)(110)(519)Cost of sales
Net Investment Hedges
Cross-currency swap
Cross-currency swap
Cross-currency swap(45,498)24,920 2,202 (22,780)Interest income
$
Three Months Ended March 31, 2023
Three Months Ended March 31, 2023
Three Months Ended March 31, 2023
Cash Flow Hedges
Cash Flow Hedges
Cash Flow Hedges
Interest rate swap
Interest rate swap
Interest rate swap$56,712 $(10,534)$3,500 $42,678 Interest expense
Cross-currency swapCross-currency swap(20,271)2,191 (3,504)(14,576)Other income (expense), net
Foreign currency forward contract
Net Investment Hedges
Net Investment Hedges
Net Investment Hedges
Cross-currency swap
Cross-currency swap
Cross-currency swap(6,914)950 2,096 (8,060)Interest income
$
Derivative Instruments not designated hedges:Designated Hedges:
During the second quarter of 2021, the Company entered into a foreign currency swap, with a notional amount of $7.3 million to mitigate the risk from fluctuations in foreign currency exchange rates associated with an intercompany loan denominated in JPY.Japanese yen. In a foreign currency swap transaction, the Company agrees with another party to exchange, at specified intervals, the difference between one currency and another currency at a fixed exchange rate, generally set at inception, calculated by reference to an agreed upon notional amount. The notional amount of each currency is exchanged at the inception and termination of the currency swap by each party. The Company subsequently paid down a portion of this swap, bringing the notional amount down to $6.4 million.$5.5 million as of March 31, 2024.
The fair value of the foreign currency swaps not designated as hedges was $1.5 million and $1.2 million as of March 31, 2024 and December 31, 2023, respectively. The following table summarizes the gains (losses) ofon derivative instruments not designated as hedges on the condensed consolidated statements of income, which was included in other income:
Dollars in thousandsDollars in thousandsThree Months Ended March 31,
20232022
Dollars in thousands
Dollars in thousandsThree Months Ended March 31,
202420242023
Foreign currency swapsForeign currency swaps55 360 
Foreign currency swaps
Foreign currency swaps
TotalTotal$55 $360 
8. STOCK-BASED COMPENSATION
As of March 31, 2023,2024, the Company had stock options, restricted stock awards, performance stock awards, contract stock awards and restricted stock unit awards outstanding under the Integra LifeSciences Holdings Corporation Fifth Amended and Restated 2003 Equity Incentive Plan (the “2003 Plan”). The 2000 and 2001 Equity Incentive Plans were terminated as of February 19, 2021, and no further awards may be issued under the plans.
20

INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
Stock options issued under the 2003 Plan become exercisable over specified periods, generally within four years from the date of grant for officers and employees, within one year from date of grant for directors which generally expire eight years from the grant date for employees, and from six to ten years for directors and certain executive officers, except in certain instances that result in accelerated vesting due to death, disability, retirement age or change in-control provisions within their grant agreements. The Company values stock option grants using the binomial distribution model. Restricted stock issued under the Plans2003 Plan vests over specified periods, generally three years after the date of grant. The vesting of performance stock issued under the Plans2003 Plan is subject to service and performance conditions.
22

INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
Stock Options
As of March 31, 2023,2024, there were approximately $5.6$4.9 million of total unrecognized compensation costs related to unvested stock options. These costs are expected to be recognized over a weighted-average period of approximately three years. There were 151,293243,964 stock options granted during the three months ended March 31, 2023.2024. For the three months ended March 31, 2023,2024, the weighted average grant date fair value for stock options granted was $21.58$15.68 per option.
Awards of Restricted Stock and Performance Stock
Performance stock and restricted stock awards generally have requisite service periods of three years, except in certain instances that result in accelerated vesting due to death, disability, retirement age provision or change in-control provisions in their grant agreements. Performance stock units are subject to graded vesting conditions based on revenue goals of the Company. The Company expenses the fair value of restricted stock awards on a straight-line basis over the requisite service period. As of March 31, 2023,2024, there was approximately $48.6 million of total unrecognized compensation costs related to these unvested awards. The Company expects to recognize these costs over a weighted-average period of approximately two years. The Company granted 346,745532,379 restricted stock awards and 161,218263,350 performance stock awards during the three months ended March 31, 2023.2024. For the three months ended March 31, 2023,2024, the weighted average grant date fair value for restricted stock awards and performance stock units granted was $53.37$36.46 and $52.87$36.22 per award, respectively.
The Company also maintains an Employee Stock Purchase Plan (the “ESPP”), which provides eligible employees with the opportunity to acquire shares of common stock at periodic intervals by means of accumulated payroll deductions. The ESPP is a non-compensatory plan based on its terms.
CEO Separation
On February 27th, 2024, the Company announced that Mr. De Witte would retire from his position as President and Chief Executive Officer and director of the Company following the completion of a succession process and entered into a letter agreement with Mr. De Witte to modify his current employment agreement and put forth the form of a post-employment consulting agreement. The Company applied modification accounting to the outstanding equity-based awards granted to Mr. De Witte as of that date, which revalued and accelerated stock-based compensation associated with equity-based awards granted to him over his expected service period to the Company. Pursuant to this letter agreement, Mr. De Witte’s unvested equity-based awards will continue to vest during his continued service period to the Company and vested stock options were modified such that they will remain exercisable until the lesser of (a) the stated term of the stock options and (b) six months following his cessation of continued service to the Company. As a result of the modifications, the Company recorded incremental stock-based compensation expense of $0.2 million during the three months ended March 31, 2024. The Company will record a total of $1.9 million in accelerated stock-based compensation expenses for the twelve months ended 2024 that would not have been recognized if Mr. De Witte had not announced his retirement from Integra.
9. RETIREMENT PLANS
The Company maintains defined benefit pension plans that cover certain employees in France, Japan, Germany and Switzerland.
Net periodic benefit costs for the Company’s defined benefit pension plans for the three months ended March 31, 2024 were $0.4 million. The components of the net periodic benefit costs other than the service cost component of $0.8 million for the three months ended March 31, 2024 are included in other income, net in the consolidated statements of operations.
Net periodic benefit costs for the Company’s defined benefit pension plans for the three months ended March 31, 2023 were $0.3 million. The components of the net periodic benefit costs other than the service cost component of $0.5 million for the three months ended March 31, 2023 are included in other income, net in the consolidated statements of operations.
Net periodic benefit costs for the Company’s defined benefit pension plans for the three months ended March 31, 2022 were $0.3 million. The components of the net periodic benefit costs other than the service cost component of $0.7 million for the three months ended March 31, 2022 are included in other income, net in the consolidated statements of operations.
21

INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
The estimated fair values of plan assets were $36.4$40.4 million and $38.1$45.7 million as of March 31, 20232024 and December 31, 2022,2023, respectively. The net plan assets of the pension plans are invested in common trusts as of March 31, 20232024 and December 31, 2022.2023. Common trusts are classified as Level 2 in the fair value hierarchy. The fair value of common trusts is valued at the net asset value based on the fair values of the underlying investments of the trusts as determined by the sponsor of the trusts. The investment strategy of the Company'sCompany’s defined benefit plans is both to meet the liabilities of the plans as they fall due and to maximize the return on invested assets within an appropriate risk profile.
Deferred Compensation Plan
The Company maintains a Deferred Compensation Plan in which certain employees of the Company may defer the payment and taxation of up to 75% of their base salary and up to 100% of bonus amounts and other eligible cash compensation.
This deferred compensation is invested in funds offered under this plan and is valued based on Level 1 measurements in the fair value hierarchy. Assets of the Company'sCompany’s deferred compensation plan are included in other current assets and recorded at fair value based on their quoted market prices. The fair value of these assets were $5.0$5.7 million and $4.7$6.1 million as of March 31, 20232024 and December 31, 2022,2023, respectively. Offsetting liabilities relating to the deferred compensation plan are included in Otherother liabilities.
10. LEASES AND RELATED PARTY LEASES
The Company leases administrative, manufacturing, research and distribution facilities, and vehicles through operating lease agreements. The Company has no finance leases as of March 31, 2023.2024. Many of the Company'sCompany’s leases include both lease (e.g., fixed payments including rent) and non-lease components (e.g., common-area or other maintenance costs). For vehicles, the Company has elected the practical expedient to group lease and non-lease components.
23

INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
Most facility leases include one or more options to renew. The exercise of lease renewal options is typically at the Company'sCompany’s sole discretion, therefore, the majority of renewals to extend the lease terms are not included in the Right of Use ("ROU"(“ROU”) assets and lease liabilities as they are not reasonably certain of exercise. The Company regularly evaluates renewal options and when they are reasonably certain of exercise, the renewal period is included in the lease term.
As most of the Company'sCompany’s leases do not provide an implicit rate, the Company uses a collateralized incremental borrowing rate based on the information available at the lease commencement date in determining the present value of the lease payments.
Total operating lease expense for the three months ended March 31, 20232024 and March 31, 20222023 was $6.0$6.3 million and $4.9$6.0 million, respectively, which includes $0.1$0.3 million, in related party operating lease expense.
Supplemental balance sheet information related to operating leases were as follows:
Dollars in thousands, except lease term and discount rateMarch 31, 2023December 31, 2022
ROU assets$146,514 $148,284 
Current lease liabilities14,792 14,624 
Non-current lease liabilities156,910 157,420 
Total lease liabilities$171,702 $172,044 
Weighted average remaining lease term (in years):
Leased facilities17.1 years16.9 years
Leased vehicles2.0 years2.0 years
Weighted average discount rate:
Leased facilities5.4 %5.4 %
Leased vehicles2.8 %2.7 %
Supplemental cash flow information related to leases for the three months ended March 31, 2023 and 2022 were as follows:
Dollars in thousandsMarch 31, 2023March 31, 2022
Cash paid for amounts included in the measurement of lease liabilities:
Operating cash flows from operating leases$4,319 $4,696 
ROU assets obtained in exchange for lease liabilities:
Operating leases$1,721 $507 
Future minimum lease payments under operating leases at March 31, 2023 were as follows:
Dollars in thousandsRelated PartiesThird PartiesTotal
Remainder of 2023$222 $15,870 $16,092 
2024296 21,086 21,382 
2025296 19,753 20,049 
2026296 17,148 17,444 
2027296 16,205 16,501 
2028296 13,951 14,247 
Thereafter246 151,206 151,452 
Total minimum lease payments$1,948 $255,219 $257,167 
Less: Imputed interest85,465 
Total lease liabilities171,702 
Less: Current lease liabilities14,792 
Long-term lease liabilities156,910 
Dollars in thousands, except lease term and discount rateMarch 31, 2024December 31, 2023
ROU assets$151,834 $156,184 
Current lease liabilities16,303 15,284 
Non-current lease liabilities170,082 166,849 
Total lease liabilities$186,385 $182,133 
Weighted average remaining lease term (in years):
Leased facilities16.5 years16.3 years
Leased vehicles2.1 years1.9 years
Weighted average discount rate:
Leased facilities5.7 %5.9 %
Leased vehicles2.7 %2.7 %
2422

INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
Supplemental cash flow information related to leases for the three months ended March 31, 2024 and 2023 were as follows:
Dollars in thousandsMarch 31, 2024March 31, 2023
Cash paid for amounts included in the measurement of lease liabilities:
Operating cash flows from operating leases$5,734 $4,319 
ROU assets obtained in exchange for lease liabilities:
Operating leases$746 $1,721 
Future minimum lease payments under operating leases at March 31, 2024 were as follows:
Dollars in thousandsRelated PartiesThird PartiesTotal
Remainder of 2024$222 $17,884 $18,106 
2025296 22,859 23,155 
2026296 20,210 20,506 
2027296 18,892 19,188 
2028296 16,603 16,899 
2029246 15,771 16,017 
Thereafter— 163,479 163,479 
Total minimum lease payments$1,652 $275,698 $277,350 
Less: Imputed interest90,965 
Total lease liabilities186,385 
Less: Current lease liabilities16,303 
Long-term lease liabilities170,082 
There were no future minimum lease payments under finance leases at March 31, 2023.2024.
Related Party Leases
The Company leases its manufacturing facility in Plainsboro, New Jersey, from Plainsboro Associates, a New Jersey general partnership. Ocirne, Inc., a subsidiary of Provco Industries, owns apartnership that is 50% % interest in Plainsboro Associates. Provco Industries is the corporate general partner of Tru St. Partnership LLP,owned by a principal stockholder of the Company. The term of the current lease agreement is through October 31, 2029 at an annual rate of approximately $0.3 million per year.million. The current lease agreement also provides (i) a 5-year renewal option for the Company to extend the lease from November 1, 2029 through October 31, 2034 at the fair market rental rate of the premises, and (ii) another 5-year renewal option to extend the lease from November 1, 2034 through October 31, 2039 at the fair market rental rate of the premises.
11. TREASURY STOCK
As of March 31, 20232024 and December 31, 2022,2023, there were 8.912.7 million and 6.812.8 million shares of treasury stock outstanding with a cost of $481.7$646.4 million and $362.9$647.3 million, at a weighted average cost per share of $54.01$50.76 and $53.18,$50.76, respectively.
On August 15, 2023, the Company entered into a $125 million accelerated share repurchase (“August 2023 ASR”) and received 2.3 million shares of common stock at inception of the August 2023 ASR, which represented approximately 80% of the expected total shares under the August 2023 ASR. On October 18, 2023 the early exercise provision was exercised by the August 2023 ASR counterparty. The Company received an additional 0.9 million shares determined using the volume-weighted average price of the Company’s common stock during the term of the August 2023 ASR.
23

INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
On January 26, 2023, the Company entered into a $150 million accelerated share repurchase ("(“January 2023 ASR"ASR”) and received 2.1 million shares of the Company common stock at inception of the January 2023 ASR, which represented approximately 80% of the expected total shares under the January 2023 ASR. The remaining repurchase transactions are expected to besettlement of the January 2023 ASR agreement was completed in the second quarter of 2023.2023, where the Company received 0.6 million shares, determined using the volume-weighted average price of the Company’s common stock during the term of the January 2023 ASR.
On August 16, 2022, the Inflation Reduction Act of 2022 (the “Act”“Inflation Act”) was signed into law. The Inflation Act implements a new excise tax of 1% on the net share repurchases made by the companyCompany effective for share repurchases performed January 1, 2023, or after.
On July 18, 2023, the Board of Directors authorized a new $225 million share repurchase program, replacing the existing $225 million program authorized in April 2022, under which $75 million remained authorized at the time of its replacement. As of March 31, 2024,$100 million remained authorized. The company accrued $1.2 million regarding the excise taxprogram authorized in Q-1 related to the ASR mentioned above.
On January 12, 2022,July 2023 allows the Company entered into a $125 millionto repurchase its shares opportunistically from time to time. The Company may utilize various methods to effect any repurchases, including open market transactions, privately negotiated transactions, transactions structured through investment banking institutions, including accelerated share repurchase ("2022 ASR") and received 1.48 million shares of Company common stock at inceptionrepurchases, or a combination of the 2022 ASR,foregoing, some of which represented approximately 80%may be effected through Rule 10b5-1 plans. The price and timing of the expected total sharesany future purchases under the 2022 ASR. On March 24, 2022,share repurchase program will depend on factors such as levels of cash generation from operations, the early exercise provision under the 2022 ASR was exercisedvolume of stock option exercises by 2022 ASR counterparty. Upon settlement on March 24, 2022, the Company received an additional 0.46 million shares determined using the volume-weighted averageemployees, cash requirements for acquisitions, dividends, economic and market conditions and stock price, of the Company's common stock during the term of the 2022 ASR.and such repurchases may be discontinued at any time.
12. INCOME TAXES
The following table provides a summary of the Company'sCompany’s effective tax rate:
 Three Months Ended March 31,
 20232022
Reported tax rate18.6 %16.3 %
 Three Months Ended March 31,
 20242023
Reported tax rate37.3 %18.6 %
The Company’s effective income tax rates for the three months ended March 31, 2024 and 2023 were 37.3% and 2022 were 18.6% and 16.3%, respectively. For the three months ended March 31, 2023, the primary driver of2024, the higher tax rate relatesis attributable to a reduction of excess tax benefits$1.5 million shortfall from stock compensation.based compensation, offset by a tax benefit for the intangible asset impairment, as compared to previous year. The Company does not have tax basis in the impaired intangible asset and has treated the tax impact as a discrete event in this quarter.
Changes to income tax laws and regulations, in any of the tax jurisdictions in which the Company operates, could impact the effective tax rate. Various governments, both U.S. and non-U.S., are increasingly focused on tax reform and revenue-raising legislation. On August 16, 2022, the Inflation Act was signed into law. The Company did not experience a material impact on the Company’s effective tax rate under the Inflation Act. Further, legislation in foreign jurisdictions may be enacted, in continued response to the base erosion and profit-sharing (“BEPS”) project begun by the Organization for Economic Cooperation and Development ("OECD"(“OECD”).
The OECD recently finalized major reform of the international tax system with respectreleased model rules related to a new 15% global minimum tax rate.regime (“Pillar 2”). Several of the jurisdictions that the Company operates in have already adopted some form of the model rules, which could impact the amount of taxes that the Company pays after 2023. However, the rules are complex and provide for delays for implementing the tax during the early transition years, if certain conditions are met. At this time, the Company is projecting an immaterial amount related to Pillar 2 tax liability for the 2024 year. Such changes in U.S. and non-U.S.Non-U.S. jurisdictions could have an adverse effect on the Company’s effective tax rate.
As of March 31, 2023, the Company has not provided deferred income taxes on unrepatriated earnings from foreign subsidiaries as they are deemed to be indefinitely reinvested unless there is a manner under which to remit the earnings with no material tax cost. Material taxes would primarily be attributable to foreign withholding taxes and local income taxes when such earnings are distributed. The Company will repatriate foreign earnings when there is no need for reinvestment overseas and there is no material cost to bring the earnings back to the United States. Reinvestment considerations would include future acquisitions, transactions, and capital expenditure plans.
2524

INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
13. NET INCOME PER SHARE
Basic and diluted net income per share was as follows:
Three Months Ended March 31,Three Months Ended March 31,
Dollars in thousands, except per share amounts Dollars in thousands, except per share amounts20232022 Dollars in thousands, except per share amounts20242023
Basic net income per share:
Net income$24,226 $32,901 
Basic net (loss) income per share:
Net (loss) income
Net (loss) income
Net (loss) income
Weighted average common shares outstandingWeighted average common shares outstanding81,871 83,632 
Basic net income per common share$0.30 $0.39 
Basic net (loss) income per common share
Basic net (loss) income per common share
Basic net (loss) income per common share
Diluted net income per share:
Net income$24,226 $32,901 
Diluted net (loss) income per share:
Diluted net (loss) income per share:
Diluted net (loss) income per share:
Net (loss) income
Net (loss) income
Net (loss) income
Weighted average common shares outstanding — Basic
Weighted average common shares outstanding — Basic
Weighted average common shares outstanding — BasicWeighted average common shares outstanding — Basic81,871 83,632 
Effect of dilutive securities:Effect of dilutive securities:
Stock options and restricted stockStock options and restricted stock452 644 
Stock options and restricted stock
Stock options and restricted stock
Weighted average common shares for diluted earnings per shareWeighted average common shares for diluted earnings per share82,323 84,276 
Diluted net income per common share$0.29 $0.39 
Diluted net (loss) income per common share
Diluted net (loss) income per common share
Diluted net (loss) income per common share
Basic earnings per share is computed by dividing net income by the weighted-average common shares outstanding during the period. Diluted earnings per share is computed based on the weighted-average common shares outstanding plus the effect of dilutive potential common shares outstanding during the period calculated using the treasury stock method. Dilutive potential common shares include employee equity share options, non-vested shares, and similar equity instruments granted by the Company. Potential common share equivalents have been excluded where their inclusion would be anti-dilutive.
Common stock of approximately 1.3 million and 0.3 million and 0.2 million shares at March 31, 2023,2024, and 2022,2023, respectively, that are issuable through exercise of dilutive securities were not included in the computation of diluted net (loss) income per share because their effect would have been anti-dilutive.
14. ACCUMULATED OTHER COMPREHENSIVE INCOME (LOSS)
Comprehensive income for the three months ended March 31, 20232024 and 2022 was as follows:2023:
 Three Months Ended March 31,
Dollars in thousands20232022
Net income$24,226 $32,901 
Foreign currency translation adjustment4,076 (5,683)
Change in unrealized loss/(gain) on derivatives, net of tax(7,377)29,822 
Pension liability adjustment, net of tax103 (9)
Comprehensive income, net$21,028 $57,031 
Changes in accumulated other comprehensive income by component between December 31, 2022 and March 31, 2023 are presented in the table below, net of tax:
Dollars in thousandsGains and Losses on DerivativesDefined Benefit Pension ItemsForeign Currency ItemsTotal
Balance at January 1, 2023$22,817 $9,322 $(21,874)$10,265 
Other comprehensive gain (loss)(5,754)103 4,076 (1,575)
Less: Amounts reclassified from accumulated other comprehensive income, net1,623 — — 1,623 
Net current-period other comprehensive gain (loss)(7,377)103 4,076 (3,198)
Balance at March 31, 2023$15,440 $9,425 $(17,798)$7,067 
For the three months ended March 31, 2023, the Company reclassified a gain of $4.3 million and a loss of $2.7 million from accumulated other comprehensive income to other income, net and interest income, respectively.
 Three Months Ended March 31,
Dollars in thousands20242023
Net (loss) income$(3,281)$24,226 
Foreign currency translation adjustment730 3,192 
Change in unrealized loss/(gain) on derivatives, net of tax3,735 (6,493)
Pension liability adjustment, net of tax(5)103 
Comprehensive income, net$1,179 $21,028 
2625

INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
Changes in accumulated other comprehensive income by component between December 31, 2023 and March 31, 2024 are presented in the table below, net of tax:
Dollars in thousandsGains and Losses on DerivativesDefined Benefit Pension ItemsForeign Currency ItemsTotal
Balance at January 1, 2024$21,489 $2,712 $(39,307)$(15,106)
Other comprehensive gain (loss)34,939 (5)2,425 37,359 
Less: Amounts reclassified from accumulated other comprehensive income, net31,204 — 1,695 32,899 
Net current-period other comprehensive gain (loss)3,735 (5)730 4,460 
Balance at March 31, 2024$25,224 $2,707 $(38,577)$(10,646)
For the three months ended March 31, 2024, the Company reclassified a gain of $27.2 million and $5.7 million from accumulated other comprehensive income to other income, net and interest income, respectively.
15. SEGMENT AND GEOGRAPHIC INFORMATION
The Company internally manages two global reportable segments and reports the results of its businesses to its chief operating decision maker. The two reportable segments and their activities are described below.
The Codman Specialty Surgical segment includes (i) the Neurosurgery business, which sells a full line of products for neurosurgery and neuro critical care such as tissue ablation equipment, dural repair products, cerebral spinal fluid management devices, intracranial monitoring equipment, and cranial stabilization equipment and (ii) the Instruments business, which sells more than 40,000 instrument patterns and surgical and lighting products to hospitals, surgery centers, dental, podiatry, and veterinary offices.
The TTTissue Technologies segment includes such offerings as skin and wound repair, plastics & surgical reconstruction products, bone grafts, and nerve and tendon repair products.
The Corporate and other category includes (i) various executive, finance, human resource, information systems and legal functions, (ii) brand management, and (iii) share-based compensation costs.
The operating results of the various reportable segments as presented are not comparable to one another because (i) certain operating segments are more dependent than others on corporate functions for unallocated general and administrative and/or operational manufacturing functions, and (ii) the Company does not allocate certain manufacturing costs and general and administrative costs to the operating segment results. Net sales and profit by each reportable segment for the three months ended March 31, 20232024 and 20222023 are as follows:
Three Months Ended March 31,
Three Months Ended March 31,
Three Months Ended March 31,
Three Months Ended March 31,
Dollars in thousandsDollars in thousands20232022Dollars in thousands20242023
Segment Net SalesSegment Net Sales
Codman Specialty Surgical
Codman Specialty Surgical
Codman Specialty SurgicalCodman Specialty Surgical$248,136 $247,308 
Tissue Technologies
Tissue Technologies
132,710 129,330 
Total revenuesTotal revenues$380,846 $376,638 
Segment ProfitSegment Profit
Codman Specialty Surgical
Codman Specialty Surgical
Codman Specialty SurgicalCodman Specialty Surgical$110,933 $110,160 
Tissue Technologies
Tissue Technologies
52,281 53,893 
Segment profitSegment profit163,214 164,053 
AmortizationAmortization(3,108)(3,894)Amortization(10,107)(3,108)(3,108)
Corporate and otherCorporate and other(123,724)(113,995)Corporate and other(120,087)(123,724)
Operating incomeOperating income$36,382 $46,164 
26

INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
The Company does not allocate any assets to the reportable segments. No asset information is reported to the chief operating decision maker and disclosed in the financial information for each segment. The Company attributes revenues to geographic areas based on the location of the customer. Total revenue by major geographic area consisted of the following:
Three Months Ended March 31,Three Months Ended March 31,
Dollars in thousandsDollars in thousands20232022Dollars in thousands20242023
United StatesUnited States$271,002 $263,351 
EuropeEurope41,064 43,744 
Asia PacificAsia Pacific50,473 47,717 
Rest of WorldRest of World18,307 21,826 
Total RevenuesTotal Revenues$380,846 $376,638 
16. COMMITMENTS AND CONTINGENCIES
In consideration for certain technology, manufacturing, distribution, and selling rights and licenses granted to the Company, the Company has agreed to pay royalties on sales of certain products that it sells. The royalty payments that the Company made under these agreements were not significant for any of the periods presented.
27

INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
The Company is subject to various claims, lawsuits and proceedings inIn the ordinary course of its business, the Company's business,Company is involved in, from time to time, various legal actions, including claims by current or former employees, distributors and competitors and with respect to its products andany matters described below, involving product liability, claims, lawsuitsemployment, intellectual property and commercial disputes, shareholder related matters, environmental proceedings, tax disputes, and governmental proceedings and investigations, some of which have been settled by the Company. In the opinion of management, such claimsmatters are either adequately covered by insurance or otherwise indemnified, or are not expected, individually or in the aggregate, to result in a material, adverse effect on the Company'sCompany’s financial condition. However, it is possible that the Company'sCompany’s results of operations, financial position and cash flows in a particular period could be materially affected by these contingencies.
The Company accrues for loss contingencies when it is deemed probable that a loss has been incurred and that loss is estimable. The amounts accrued are based on the full amount of the estimated loss before considering insurance proceeds and do not include an estimate for legal fees expected to be incurred in connection with the loss contingency. The Company consistently accrues legal fees expected to be incurred in connection with loss contingencies as those fees are incurred by outside counsel as a period cost.
On December 21, 2023, Fortis Advisors, LLC (representative of the security holders of ACell, Inc. (“ACell”)) filed for arbitration against Integra Life Sciences claiming breach of contract related to the earnout consideration from the 2021 acquisition of ACell. Refer below for additional information on the ACell contingent considerations. The Company believes that it has strong defenses to the allegations in the arbitration and intends to defend the matter vigorously.
On September 12, 2023, a securities class action complaint, captioned Pembroke Pines Firefighters & Police Officers Pension Fund v. Integra LifeSciences Holdings Corporation, No. 23-cv-20321 (D.N.J.), was filed by a purported stockholder of the Company in the United States District Court for the District of New Jersey (the “Pembroke Litigation”) against the Company and certain of the Company’s current and former executive officers. The Pembroke Litigation, filed on behalf of a putative class of stockholders who purchased or acquired the Company’s common stock between March 11, 2019 and May 22, 2023, inclusive, alleges violations of Sections 10(b) and 20(a) of the Securities Exchange Act of 1934, as amended, and Rule 10b-5 promulgated thereunder, on the basis of purportedly materially false and misleading statements and omissions relating to certain quality systems issues identified by the U.S. Food and Drug Administration at the Company’s Boston, Massachusetts manufacturing facility, the Company’s efforts to remediate those issues, and the Company’s forecasts for certain products in its Tissue Technologies segment. The complaint seeks, among other things, compensatory damages, attorneys’ fees, expert fees, and other costs. The Company believes that it has strong defenses to the allegations in the Pembroke Litigation, and intends to defend the matter vigorously.
Contingent Consideration
The Company determined the fair value of contingent consideration during the three month period ended March 31, 20232024 and March 31, 20222023 to reflect the change in estimate, additions, payments, transfers and the time value of money during the period.
27

INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
A reconciliation of the opening balances to the closing balances of these Level 3 measurements for the three months ended March 31, 20232024 and March 31, 20222023 is as follows (in thousands):
Three Months Ended March 31, 2023Contingent Consideration Liability Related to Acquisition of:
ArkisLocation in Financial StatementsDerma SciencesACellSurgical Innovations Associates, Inc. (FN 2)Location in Financial Statements
Short-termLong-termLong-termLong-termShort-termLong-term
Balance as of January 1, 2023$2,845 $10,050 $230 $3,700 $— $57,607 
Transfers— — — — 12,500 (12,500)
Change in fair value of contingent consideration liabilities1,543 1,756 Research and development— (2,200)— 3,600 Selling, general and administrative
Balance as of March 31, 20234,388 11,806 230 1,500 12,500 48,707 
Three Months Ended March 31, 2024Contingent Consideration Liability Related to Acquisition of:
ArkisLocation in Financial StatementsDerma SciencesACellSurgical Innovations Associates (SIA), Inc.Location in Financial Statements
Balance as of January 1, 2024$15,755 $2,557 $300 68,700 
Change in fair value of contingent consideration liabilities(83)Research and development39 — 500 Selling, general and administrative
Balance as of March 31, 202415,672 2,596 300 69,200 
Short-Term$7,562 $— $— $29,300 Accrued expenses and other current liabilities
Long-Term8,110 2,596 300 39,900 Other liabilities
Total15,672 2,596 300 69,200 
Three Months Ended March 31, 2022Contingent Consideration Liability Related to Acquisition of:
ArkisLocation in Financial StatementsDerma SciencesACell Inc.Location in Financial Statements
Short-termLong-termLong-termShort-termLong-term
Balance as of January 1, 2022$3,691 $11,408 $230 $— $21,800 
Transfers59 (59)— 4,885 (4,885)
Change in fair value of contingent consideration liabilities— (1,065)Research and development— — 300 Selling, general and administrative
Balance as of March 31, 2022$3,750 $10,284 $230 $4,885 $17,215 
28

INTEGRA LIFESCIENCES HOLDINGS CORPORATION
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
Three Months Ended March 31, 2023Contingent Consideration Liability Related to Acquisition of:
ArkisLocation in Financial StatementsDerma SciencesACellSurgical Innovations Associates (SIA), Inc.Location in Financial Statements
Balance as of January 1, 2023$12,895 $230 $3,700 $57,607 
Change in fair value of contingent consideration liabilities3,299 Research and development— (2,200)3,600 Selling, general and administrative
Balance as of March 31, 2023$16,194 $230 $1,500 $61,207 
Short-Term$4,388 $— $— $12,500 Accrued expenses and other current liabilities
Long-Term11,806 230 1,500 48,707 Other liabilities
Total16,194 230 1,500 61,207 
Arkis BioSciences Inc.
As part of the acquisition of Arkis BioSciences Inc. ("Arkis"(“Arkis”), the Company is required to pay the former shareholders of Arkis up to $25.5 million based on the timing of certain development milestones of $10.0 million and commercial sales milestones of $15.5 million, respectively. The Company used a probability weighted income approach to calculate the fair value of the contingent consideration that considered the possible outcomes of scenarios related to each specified milestone. The Company estimated the fair value of the contingent consideration to be $13.1 million at the acquisition date. The estimated fair value as of March 31, 2023 and March 31, 2022 was $16.2 million and $14.0 million, respectively. The Company recorded $11.8 million and $10.3 million in other liabilities at March 31, 2023 and March 31, 2022, respectively, and $4.4 million and $3.8 million in accrued expenses and other current liabilities at March 31, 2023 and March 31, 2022, respectively, in the consolidated balance sheet of the Company.
Derma Sciences, Inc.
The Company assumed contingent consideration incurred by Derma Sciences, Inc. ("(“Derma Sciences"Sciences”) related to its acquisitions of BioD, LLC and the intellectual property related to MedihoneyMedihoney® products. The Company accounted for the contingent liabilities by recording theirthe fair value on the date of the acquisition based on a probability weighted income approach. The Company has already paid $33.3 million related to the aforementioned contingent liabilities. One contingent milestone remains which relates to net sales of Medihoney™Medihoney®™ products exceeding certain amounts defined in the agreement between the Company and Derma Sciences. The potential maximum undiscounted payment amounts to $3.0 million. The estimated fair value as of March 31, 2023 and March 31, 2022 was $0.2 million.

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NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (continued)
ACell, Inc.
As part of the acquisition of ACell, Acquisition, the Company is required to make payments to the former shareholders of ACell up to $100 million in total for years 2022, 2023, and 2025 based on the achievement by the Company of certain revenue-based performance milestones. The 2022 and 2023 milestones in 2023 and 2025.were not achieved, leaving only one contingent milestone remaining. The Company used iterations of the Monte Carlo simulation to calculate the fair value of the contingent consideration that considered the possible outcomes of scenarios related to each specific milestone. The Company estimated the fair value of the contingent consideration to be $23.9$23.9 million at the acquisition date. The estimated fair value
Surgical Innovations Associates, Inc.
As part of the acquisition of Surgical Innovations Associates, Inc. (“SIA”), the Company is required to pay to the former shareholders of SIA up to $90.0 million for two separate payments, which are dependent on 1) achieving certain revenue-based performance milestones in 2023, 2024, and 2025 (up to $50.0 million in additional payments), as well as 2) the approval by the FDA of March 31, 2023 was $1.5the PMA for DuraSorb for certain uses by certain timing targets (up to $40.0 million in additional payments). The Company recorded $1.5 million and $17.2 million in other liabilities at March 31, 2023 and March 31, 2022, respectively, and $4.9 million in accrued expenses and other current liabilities at March 31, 2022 in the consolidated balance sheetsused iterations of the Company. The change inMonte Carlo simulation to calculate the fair value of the contingent obligation was primarily as a resultconsideration for the revenue-based milestone that considered the possible outcomes of changes inscenarios related to each specific milestone for the timingrevenue based performance milestone. The Company used probabilities of achieving the conditions to calculate the fair value of the contingent consideration for the PMA approval milestone. The Company estimated the fair value of the contingent consideration for the revenue based milestone to be $32.6 million at the acquisition date and amount of revenue estimates.$25.0 million for the PMA approval milestone at the acquisition date.


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ITEM 2. MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS
The following discussion and analysis of the Company'sCompany’s financial condition and results of operations should be read in conjunction with our unaudited condensed consolidated financial statements and the related notes thereto appearing elsewhere in this reportQuarterly Report on Form 10-Q (this “Quarterly Report”) and our consolidated financial statements for the year ended December 31, 2022 included in our Annual Report on Form 10-K.

10-K for the year ended December 31, 2023.
We have made statements in this reportQuarterly Report that constitute forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended and Section 21E of the Securities Exchange Act of 1934 (the “Exchange Act”). All statements other than statements of historical fact contained in this Quarterly Report, on Form 10-Q (this “Quarterly Report”), including, but not limited to, statements regarding our future results of operations and financial position, business strategy and plans, objectives of management for future operations and current expectations or forecasts of future results, are forward-looking statements. These forward-looking statements are subject to a number of risks, uncertainties and assumptions about the Company and other matters that may cause our actual results, performance, or achievements to be materially different from any future results, performance, or achievements expressed or implied by the forward-looking statements.

These statements involve known and unknown risks, uncertainties, and other important factors that may cause our actual results, performance, or achievements to be materially different from any future results, performance, or achievements expressed or implied by the forward-looking statements. Our forward-looking statements may include statements related to our growth and growth strategies, developments in the markets for our products and services, financial results, development launches and effectiveness, research and development strategy, regulatory approvals, competitive strengths, the potential or anticipated direct or indirect impact of the Coronavirus pandemic on our business, results of operations, and/or financial condition, objectives of management for future operations and current expectations or forecasts of future results, our expectations regarding the Boston facility; restructuring and cost-saving initiatives, intellectual property rights, litigation and tax matters, governmental proceedings and investigations, mergers and acquisitions, divestitures, market acceptance of our products and services, accounting estimates, financing activities, ongoing contractual obligations, working capital adequacy, value of our investments, our effective tax rate, our expected returns to shareholders, and sales efforts.

efforts, are forward-looking statements. In some cases, these forward-looking statements may be identified by forward-looking words such as “believe,” “may,” “might,” “could,” “will,” “estimate,” “continue,” “anticipate,” “intend,” “seek,” “plan,” “expect,” “should,” “would” andor the negative version of these words or other similar words and expressions in this report. Forward-lookingQuarterly Report.
These forward-looking statements in this Quarterly Reportare subject to a number of risks, uncertainties and assumptions about the Company and other matters that may cause our actual results, performance, or achievements to be materially different from any future results, performance, or achievements expressed or implied by the forward-looking statements. We believe these risks include but are not limited to statements regardingthose described under the headings “Risk Factors” and “Special Note Regarding Forward-Looking Statements” in our Annual Report on Form 10-K for the year ended December 31, 2023 and in this Quarterly Report, as such factors may be updated from time to time in our periodic filings with the Securities and Exchange Commission (the “SEC”), which are accessible on the SEC’s website at https://www.sec.gov. Such risks and uncertainties include, but are not limited, to the following: the ongoing and possible future effects of global challenges, including macroeconomic uncertainties, inflation, supply chain disruptions, trade regulation and tariffs, other economic disruptions and U.S. and global recession concerns, on the Company’s customers and on the Company’s business, financial condition, results of operations and cash flows; the Company's ability to drive long-term shareholder value, developmentexecute its operating plan effectively; the Company’s ability to successfully integrate acquired businesses; the Company’s ability to achieve sales growth in a timely fashion; the Company’s ability to manufacture and future launchesship sufficient quantities of its products to meet its customers’ demands; the ability of third-party suppliers to supply us with raw materials and finished products; global macroeconomic and political conditions, including the war in Ukraine and the conflict in Israel and Gaza; the Company’s ability to manage its direct sales channels effectively; the sales performance of third-party distributors on whom the Company relies to generate revenue for certain products and continued or future acceptance of products and services in our segments; ourgeographic regions; the Company’s ability to navigateaccess and mitigate any on-goingmaintain relationships with customers of acquired entities and businesses; physicians’ willingness to adopt and third-party payors’ willingness to provide or future impact associatedmaintain reimbursement for the Company’s recently launched, planned and existing products; initiatives launched by the Company's competitors; downward pricing pressures from customers; the Company's ability to secure regulatory approval for products in development; the Company’s ability to remediate quality systems violations; fluctuations in hospitals’ spending for capital equipment; the Company’s ability to comply with economic disruptions,regulations regarding products of human origin and products containing materials derived from animal source; difficulties in controlling expenses, including supply chain constraintscosts to procure and inflation; expected timing for completion of research studies relating tomanufacture our products; market positioningthe impact of changes in management or staff levels; the impact of goodwill and performanceintangible asset impairment charges if future operating results of acquired businesses are significantly less than the results anticipated at the time of the acquisitions, the Company’s ability to leverage its existing selling organizations and administrative infrastructure; the Company’s ability to increase product sales and gross margins, and control non-product costs; the Company’s ability to achieve anticipated growth rates, margins and scale and execute its strategy generally; the amount and timing of divestiture, acquisition and integration-related costs; the geographic distribution of where the Company generates its taxable income; new U.S. and foreign government laws and regulations, and changes in existing laws, regulations and enforcement guidance, which affect areas of our products; divestitures andoperations including, but not limited to, those affecting the potential benefits thereof; the costs and benefits of integrating previous acquisitions; anticipated timing for Food and Drug Administration (“FDA”) in the U.S., as well as for non-U.S. regulatory approval of new products; increased presence in new markets, including markets outside the U.S.; changes in the market and our market share; acquisitions and investment initiatives,health care industry, including the timingEU Medical Devices Regulation; the scope, duration and effect of additional U.S. and international governmental, regulatory, approvals as well as integration of acquired companies into our operations;fiscal, monetary and public health responses to public health crises; fluctuations in foreign currency exchange rates; the resolution of tax matters; the effectivenessamount of our development activities in reducing patient care costsbank borrowings outstanding and hospital stay lengths; our approach towards cost containment; our expectations regarding healthcare costs; general economic conditions;other factors influencing liquidity; potential negative impacts resulting from environmental, social and governance matters; and the potential impact of our compliance with governmental regulations and accounting guidance.
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We have based these forward-looking statements largely on our current expectations and projections about future events and financial trends that we believe may affect our business, results of operations, financial condition, and/or cash flows. These forward-looking statements speak only as of the date of this Quarterly Report and are subjectwe undertake no obligation to a number of risks, uncertainties and assumptions described in the “Risk Factors” section and elsewhere in our Annual Report on Form 10-K for the year ended December 31, 2022. Aspublicly update or revise any forward-looking statements, are inherently subjectwhether as a result of new information, future events or otherwise, except to risks and uncertainties, some of which cannot be predicted or quantified, youthe extent required by applicable law. You should not rely on these forward-looking statements as predictions of future events. One must carefully consider forward-looking statements and understand that such forward-looking statements are inherently subject to risks and uncertainties, some of which cannot be predicted or quantified, and involve a variety of risks and uncertainties, known and unknown, including, among others, those discussed in the sections entitled “Government Regulation” within “Item 1. Business” and “Item 1A. Risk Factors” in our Annual Report on Form 10-K for the year ended December 31, 2022. We undertake no obligation to publicly update or revise any forward-looking statements, whether as a result of new information, future events or otherwise, except to the extent required by applicable law.uncertainties.

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GENERAL
Integra, headquarteredWe are a leading global medical technology company innovating treatment pathways in Princeton, New Jersey, is a world leader in neurosurgical solutionssurgical, neurologic and regenerative tissue technologies. The Company was foundedcare to advance patient outcomes and set new standards of surgical, neurologic and regenerative care. Founded in 1989 with the acquisition of an engineered collagen technology platform used to repair and regenerate tissue. Integra hastissue, our common stock trades on the Nasdaq Global Select Market (“Nasdaq”) under the symbol “IART.” We have developed numerous product lines from this technology for applications ranging from burn and deep tissue wounds to the repair of dura mater in the brain, as well as nerves and tendons. We have expanded our base regenerative technology business to include surgical instruments, neurosurgical products and advanced wound care through global acquisitions and product development to meet the evolving needs of itsour customers and enhance patient care. Integra LifeSciences Holdings Corporation common stock trades on the Nasdaq Global Select Market (“Nasdaq”) under the symbol “IART.”
Our products are sold in more than 120 countries through a direct sales force as well as distributors and wholesalers. We manufacture and sell medical technologies and products in two reportable business segments: Codman Specialty Surgical ("CSS"(“CSS”) and Tissue Technologies ("TT"(“TT”). The CSS segment, which represents approximately two-thirds of our total revenue, consists of market-leading technologies and instrumentation used for a wide range of specialties, such as neurosurgery, neurocritical care and otolaryngology. We are the world leader in neurosurgery and one of the top three providers in instruments used in precision, specialty, and general surgical procedures. Our TT segment generates about one-third of our overall revenue and focuses on three main areas: complex wound surgery, surgical reconstruction, and peripheral nerve repair.
We have key manufacturing and research facilities located in California, Indiana, Maryland, Massachusetts, New Jersey, Ohio, Puerto Rico, Tennessee, Utah, France, Germany, Ireland and Switzerland. We source most of our handheld surgical instruments and dural sealant products through specialized third-party vendors.

Integra is committed to restoring patients’ lives through transformative technologies and products in the segments in which we compete. Our mission is to innovate treatment pathways to advance patient outcomes and set new standards of care. We refocused our strategies are focused around five pillars. Of these five pillars, specificallywe have identified three core growth drivers --drivers: (1) innovating for outcomes, (2) growing internationally, and (3) broadening our impact on care pathways –pathways. Our execution of the core growth drivers is enabled by two key levers: (4) driving operational and customer excellence and (5) cultivating a high-performance culture. TheseAs outlined in greater detail below, we believe these five pillars drive howwill enable us to realize and where we aimadvance our integrated growth strategy.
To this end, our executive leadership team has established the following key priorities aligned to accelerate in 2023 and in the coming years.

following five pillars:
Innovating for Outcomes. An important part of Integra’s growth strategy is introducing new products to strengthen and expand our portfolio.portfolio, including via acquisitions. For example, On April 1, 2024, the Company successfully completed the acquisition of Acclarent from Ethicon, Inc., a subsidiary of Johnson & Johnson. Acclarent is an innovator and market leader in ear, nose and throat (“ENT”) procedures and we believe that the acquisition of Acclarent will provide Integra with the opportunity to become a leading provider of ENT products and technologies. Furthermore, we believe that, owing to the ENT segment being an anatomical adjacency to neurosurgery, the acquisition will allow Integra to deliver future innovation both within the ENT segment and across our other CSS technology platforms. Additionally, we seek clinical evidence to support regulatory approval and strong reimbursement of our product portfolio around the world, including new indications for existing technologies. On December 6,For example, in 2021, we filed a pre-market approval (“PMA”) application for a specific indication for Surgimend® in the use of post-mastectomy breast reconstruction. In 2022, we completed the acquisition of Surgical Innovation Associates, Inc. (“SIA”),acquired SIA, which develops, markets and sellsis also pursuing a PMA for DuraSorb a resorbable synthetic matrix for plastic and reconstructive surgery. This acquisition advances our global strategy in breast reconstruction, expanding plans to access the U.S. market where SIA is pursuing pre-market approval for use in implant-based breast reconstruction ("IBBR"(“IBBR”)., and in June 2023 we completed enrollment in the DuraSorb U.S. investigational device exemption clinical study for two-stage breast reconstruction; the primary follow-up period is one year after device implantation. We hope to have approval for DuraSorb in 2025. For SurgiMend, we are not currently able to predict an approval date because of the delays in remediating our Boston manufacturing site. We also continued to advance the development of pioneering neurosurgical technologies with the expansion of our product offerings. In early 2023 we launched the CUSA® Clarity Bone Tip was launchedTips for use in U.S., which is used whensurgical procedures requiring the controlled fragmentation, emulsification and aspiration of bone is necessary. This follows the CUSA® Clarity extended laparoscopic tip, launchedas well as in the U.S. in late 2022 to enhance the benefits of ultrasonic ablation to minimally invasive laparoscopic liver surgery.

Growing International.Internationally: Over the years, we have been significantly expanding our global footprint through investments in our commercial organization,and manufacturing organizations, the expansion and development of international markets and new product introductions. As part of our In-China-For-China strategy, we continue the build out of our assembly capabilities in our new facility in Suzhou, China. Several new products were introduced in select international markets in 2023, including MicroMatrix® and Certas Plus® Programmable Valve which were launched in Europe, and CUSA Clarity Laparoscopic ("Lap") tip
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which was launched in Australia, New Zealand, Japan, Canada, South Africa and New Zealand.

Israel. In addition, DuraGen Secure, received approval in Japan, while DuraGen Plus, an absorbable and sutureless collagen onlay indicated as a dura substitute for the repair of dura mater, was approved in China.
Broadening Impact on Care Pathways. Integra seeksWe seek ways to develop products and technologies that impact the lives of patients, starting with the journey that a patient takes from diagnosis and treatment planning to surgery and postoperative care. Integra isWe are well-established in acute care in the hospital setting and planscontinue to leverage that strong position to grow in this segment and shape treatment pathways into preoperative care and additional sites of care.

Driving Operations and Customer Excellence. Integra hasWe have been making investments to build more responsive and scalable processes, enhance the reliability of our supply chain, and drive productivity initiatives to further supply and lower costs. Additionally, we continue to invest in technologies, systems and processes to enhance the customer experience. In 2022, certain transactional back-office financeWe continue to invest in our capacity expansion. This includes ongoing projects of transferring our Boston manufacturing to a new location in Braintree, Massachusetts, validating manufacturing processes in our manufacturing facility in Plainsboro, New Jersey and customer service activities were outsourced to enhance customer quality, build scale for future growth, and capture cost efficiencies.

increasing cleanroom capacity in our Memphis, Tennessee location.
Cultivating a High-Performance Culture. CreatingIn seeking to sustain a culture of excellence and accountability, we have focused on employee empowerment and agility and building a diverse and inclusive workplace are cornerstones of our people strategy.workplace. These efforts resulted in Integraour being named in several best workplace lists globally in 2022. Most recently, Integra China was recognized as a Great Place to Work in Greater China.
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2023. Additionally, we have been making greatfurther strides in advancing our environmental, social and governance ("ESG"(“ESG”) agenda to drive sustainability across the organization and recently published our firstsecond annual ESG report in late 2022.the third quarter of 2023. For more information on our ESG strategy, goals, performance, and achievements, please visit “Our Company—ESG Report” at https://www.integralife.com/esg-report. Information on our website is not incorporated by reference herein and is not part of this Quarterly Report.
ClinicalNew Product Introductions and ProductResearch and Development ActivitiesUpdates
Integra continuesWe continue to invest in collecting clinical evidence to support our existing products and new product launches, and to ensure that we obtain market access for broader and more cost-effective solutionssolutions.
In 2022,Electromechanical Technologies and Instrumentation. The CSS business consists of a broad portfolio of market-leading brands, such as Codman®, DuraGen®, DuraSeal®, CUSA®, Mayfield®, Bactiseal®, and Certas® Plus, which are used for the management of multiple disease states, including brain tumors, traumatic brain injury, hydrocephalus and other neurological conditions. The growth in this business in recent years has been fueled by geographic expansion and new product registrations in markets, such as China, Japan, and Europe, which we expect to continue in the near-to-long term. Because our electromechanical products and instruments address significant needs in surgical procedures and limit uncertainty for surgeons, we continue to invest in registrations, clearances, and approvals for new indications and next generation improvements to our market-leading products. We have several active programs focused on life cycle management and innovation for capital and disposable products in our portfolio. Our product development efforts are focused on core clinical applications in cerebrospinal fluid (“CSF”) management, neuro-critical care monitoring, minimally invasive instruments and electrosurgery and ultrasonic medical technologies, as well as our ambition to transform the standard of care in neurosurgery with product advancements in minimally invasive surgery (“MIS”) and the surgical management of intracerebral hemorrhage (“ICH”). Our lighting franchise is among the most dynamic in the industry.
We are focused on the development of core clinical applications in our electromechanical technologies portfolio. We continue to update our CUSA Clarity platform by incorporating new ultrasonic handpiece and integrated electrosurgical capabilities. We have made progress to several enhancements to our CUSA Clarity Tissue Ablation System. The extended laparoscopic tip was launched in the U.S. to enhance laparoscopic liver procedures. In addition, a single-sided bone tip received 510(k) clearance.clearance from the FDA. Commercial launch was completed successfully in early 2023. In earlyAugust 2023, we had our commercial launchlaunched a modified 23 kHz CUSA Electrosurgery Module (“CEM”) for Clarity handpieces that can be used with initial surgeries successfully completed.additional electrosurgery generators. We continue to update our CUSA Clarity platform by incorporatingwork with several instrument partners to bring new ultrasonic handpiece and integrated electrosurgical capabilities.surgical instrument platforms to the market.
In 2022, weWe also continued to advance the early-stage technology platforms we acquired in 2019. Through the acquisition of Arkis Biosciences, Inc. ("Arkis"(“Arkis”) we added a platform technology, CerebroFlo® external ventricular drainage ("EVD"(“EVD”), a catheter with Endexo® technology, a permanent additive designed to reduce the potential for catheter obstruction due to thrombus formation. The CerebroFlo EVD Cathetercatheter has demonstrated an average of 99% less thrombus accumulation onto its surface, in vitro, compared to a market leading EVD catheter. Our work to combine our bactisealBactiseal® antimicrobial technology with the Endexo anti-occlusive technology obtained through our 2019 acquisition of Arkis continues to progress for both a silicone-based hydrocephalus and EVD project.

In 2019, weWe also acquiredcontinued to advance our innovation from the Rebound Therapeutics Corporation ("(“Rebound Therapeutics"Therapeutics”), which was acquired in 2019. Rebound Therapeutics specializes in a company that specialized in single-use medical device, known as the Aurora Surgiscope, which is the only tubular retractor system designed for cranial surgery with an integrated access channel, camera and lighting. The 9mm Surgiscope received 510(k) clearance from the FDA in the fourth quarter of 2023.
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On August 18, 2022, the Company, after consultation with the FDA and other regulatory authorities outside of the United States, initiated an immediate voluntary global product removal of all CereLink® intracranial pressure monitors. Shipments of CereLink monitors to international markets resumed in the third quarter of 2023 and shipments in the U.S. resumed in the first quarter of 2024.
Regenerative Technologies. We were the first company to receive an FDA claim for regeneration of dermal tissue and are a world leader in regenerative technology. Our regenerative technology development program applies our expertise in bioengineering to a range of biomaterials including natural materials such as purified collagen, intact human or animal tissues, honey as well as resorbable synthetic polymers with our DuraSorb and DuraSeal product lines. These unique product designs are used for neurosurgical and reconstructive surgical applications, as well as dermal regeneration, including the healing of chronic and acute wounds, tendon and nerve repair. Our regenerative technology platform includes our legacy Integra® Dermal Regeneration Template (“IDRT”) products and complementary technologies that we have acquired. Our collagen manufacturing capability, combined with our history of innovation, including our launch of NeuraGen 3D, provides us with strong platform technologies for multiple indications.
In the second quarter of 2023, after consultation with the FDA, The Company initiated a voluntary global recall of all products manufactured at the Boston facility, including PriMatrix®, SurgiMend®, Revize™, and TissueMend™, distributed between March 1, 2018 and May 22, 2023.
In the third quarter of 2021, we conductedfiled a limited clinical launchPMA application for a specific indication for Surgimend® in the use of the Aurora Surgiscope for use in minimally invasive neurosurgery as well as initiated a registry called MIRROR to collect data on early surgical intervention using this same technology platform for the treatment of ICH.post-mastectomy breast reconstruction. In 2022, we launched the Aurora® Evacuatoracquired SIA, which has also submitted a PMA application for DuraSorb with Coagulation deviceIBBR, and in June 2023 we completed enrollment in the DuraSorb U.S., designed IDE clinical study for two-stage breast reconstruction; the primary follow-up period is one year after device implantation. By offering two distinct product solutions, we believe we have the opportunity to be used in conjunction with our Aurora Surgiscope to safely address and evacuate bloodbuild a leading position in the brain caused by hemorrhagic stroke. 
IBBR market. We hope to have approval for DuraSorb in 2025. For SurgiMend, we are focused on the development of core clinical applications in our electromechanical technologies portfolio. In June 2022, we launched the Neutus® EVD system, our first EVD in China. The Neutus EVD system is manufactured in China by Shanghai Haoju Medical Technology Co., Ltd. undernot currently able to predict an exclusive distribution arrangement. The device is used in the management of CSF and is highly complementary to our Bactiseal® catheter and advanced intercranial pressure monitoring products. In 2021, we launched our CereLink ICP Monitor System in the U.S. and Europe direct markets and continued the global rollout in the first half of 2022. CereLink provides enhanced accuracy, usability and advanced data presentation that provides clinicians with uncompromised, advanced continuous ICP monitoring that until now, has not been available when treating patients with traumatic brain injuries. Refer below to the information appearing in the "FDA Matters" section for additional information on the voluntary recallapproval date because of the CereLink ICP Monitor System.delays in remediating our Boston manufacturing site.
Within our TT segment,Additionally, in 2022 we launched NeuraGen 3D Nerve Guide Matrix, a resorbable implant for repair of peripheral nerve discontinuities and engineered to create an optimized environment for nerve regeneration. Following the completion of design control activities in 2022, we launched both Cytal and MicroMatrix in Europe in 2023. In 2023, the third quarter of 2021, we filedCompany received 510(k) clearance from the PMA applicationFDA for a specific indication for SurgiMendMicroMatrix® Flex, which is now commercially available in the useU.S. as of post-mastectomy breastMarch 2024.
As part of our ongoing efforts to remain compliant, the Company continues to work towards European Union Medical Device Regulation (“EU MDR”) certifications. In 2023 the Company received EU MDR certification in the CSS segment for Hakim Programmable Valves, Certas Plus without Bactiseal catheters, and DuraSeal Dural. Additionally, the Company received EU MDR certification in the TT segment for IDRT and BioPatch in 2023, and MicroMatrix and Cytal in 2024.
FDA Matters
On March 7, 2019, TEI Biosciences, Inc. (“TEI”), one of our wholly-owned subsidiaries, received a Warning Letter (the “2019 Warning Letter”), dated March 6, 2019, from the FDA. The 2019 Warning Letter related to quality systems issues at TEI’s manufacturing facility located in Boston, Massachusetts. The Boston facility manufactures extracellular bovine matrix products in our TT segment that are sold both in wound reconstruction and care and in private label channels. The letter resulted from an inspection held at that facility in October and November 2018 and did not identify any new observations that were not already provided in the Form 483 that followed the inspection. We submitted our initial response to the 2019 Warning Letter on March 28, 2019 and provide regular progress reports to the FDA as to its corrective actions. On October 28, 2021, the FDA initiated an inspection of the facility and at the conclusion of the inspection, issued an FDA Form 483 on November 12, 2021 (the “2021 Form 483”). We provided an initial response to the inspection observations. On March 1, 2023, the FDA commenced an inspection of the Boston facility, and issued an FDA Form 483 at the conclusion of this inspection (the “2023 Form 483”). In May 2023, after consultation with the FDA, the Company initiated a voluntary recall of products manufactured in the Boston facility distributed between March 1, 2018 and May 22, 2023, and extended the temporary halt of manufacturing at the facility to implement additional detection and quality controls. On July 19, 2023, TEI received a Warning Letter, dated July 17, 2023, from the FDA related to quality system issues at the Boston facility (the “2023 Warning Letter”). The 2023 Warning Letter did not identify any new observations that had not already been provided in the 2023 Form 483. The Company has submitted periodic responses to the FDA for both the 2023 Form 483 and the 2023 Warning Letter. We are committed to resolving the matters identified in the Warning Letters and Form 483s and are continuing our significant efforts to remediate the observations.
Although the Warning Letters do not restrict the Company’s ability to seek FDA 510(k) clearance of products, PMAs for Class III devices to which the quality system regulation violations are reasonably related will not be approved until the violations have been addressed. We cannot give any assurances that the FDA will be satisfied with our response to the issues identified by the FDA or as to the expected date of the resolution of such issues. Until the issues cited by the FDA are resolved to the FDA’s satisfaction, the FDA may initiate additional regulatory action without further notice. Any adverse regulatory
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action, depending on its magnitude, may restrict us from effectively manufacturing, marketing and selling our products and could have a material adverse effect on our business, financial condition and results of operations.
As required by the 2023 Warning Letter, we hoperetained an outside expert consultant to obtain FDA approvalperform an audit of the Boston facility in March 2024. While we anticipated this audit would yield findings and there would be remaining work to be completed, the audit yielded more findings than we anticipated. We are still determining the full scope of the work required to address these additional findings and resume commercial distribution. Based on a preliminary assessment of the work to be done, we no longer expect to resume commercial distribution in 2024. OnAs a result, the Company elected to perform impairment testing on certain definite-lived intangibles and goodwill. For further detail on the impairment testing, see Note 5. Goodwill and Other Intangible Assets.
We continue to work with our customers in wound reconstruction and care as we move toward commercialization. Revenues of products manufactured in the Boston facility for the year ended December 6,31, 2022 we completed the acquisitionwere approximately 5.3% of SIA, which develops, markets and sells DuraSorb®, a resorbable synthetic matrix for plastic and reconstructive surgery. This acquisition advances our global strategy in breast reconstruction, expanding plans to access the U.S. market where SIA is pursuing pre-market approval for use in IBBR.

FDA Mattersconsolidated revenues.
On August 18, 2022, we, after consultation with the FDA and other regulatory authorities outside of the United States, initiated an immediate voluntary global product removal of all CereLink intracranial pressure monitors as a result of customer reports about monitors whose pressure readings were out of range. We believe thatsubmitted a traditional 510(k) premarket notification to the out-of-range readings are principally caused by electrical interferenceFDA on September 15, 2023 and received 510(k) clearance on February 4, 2024 from the external environment and/or interference from a component on the circuit board of the monitor. These out-of-range readings have occurred at a low incidence rate and at a limited number of sites; however, out of an abundance of caution, we removed all CereLink monitors from the field.

We are continuing our investigation into the matter in orderFDA. The submission included design changes to remedy the observed issue and plans to resume shipmentout-of-range readings. Shipments of the CereLink monitors as soon as any such issues have been resolved and required regulatory reviews have been completed. Based onin the outlook for returning the product to market and feedback from customers, we recorded a $1.9 million provision for product returns, as a reduction of net revenue, and a $0.8 million rework accrualU.S. resumed in cost of goods sold in 2022. In the first quarter of 2023 we recorded an additional $0.8M in provision for product returns as a reduction of net revenue,2024 and no additional rework costs.
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On March 7, 2019, TEI Biosciences, Inc. ("TEI"), one of our wholly-owned subsidiaries , received a Warning Letter (the “Warning Letter”), dated March 6, 2019, from the FDA. The warning letter relatedshipments to quality systems issues at TEI's manufacturing facility located in Boston, Massachusetts. The letter resulted from an inspection held at that facility in October and November 2018 and did not identify any new observations that were not already providedinternational markets resumed in the Form 483 that followed the inspection. We submitted our initial response to the FDA Warning Letter on March 28, 2019third quarter of 2023.
Optimization and provide regular progress reports to the FDA as to its corrective actions and, since the conclusion of the inspection, we have undertaken significant efforts to remediate the observations and continue to do so. On October 28, 2021 the FDA initiated an inspection of the facility and at the conclusion of the inspection issued a FDA Form 483 on November 12, 2021 (the "2021 Form 483"). We provided an initial response to the inspection observations and will continue to provide responses to the FDA. On March 1, 2023, the FDA commenced an inspection of the facility, and we anticipate that the FDA will issue an FDA Form 483 at the conclusion of this inspection. The Warning Letter and the 2021 FDA Form 483 do not restrict our ability to manufacture or ship products or require the recall of any products, nor do they restrict our ability to seek FDA 510(k) clearance of products. Additionally, premarket approval applications for Class III devices to which the Quality System regulation violations are reasonably related will not be approved until the violations have been corrected. The TEI Boston facility manufactures extracellular bovine matrix products. We cannot give any assurances that the FDA will be satisfied with our response to the Warning Letter or as to the expected date of the resolution of the matters included in the letter. Until the issues cited in the letter are resolved to the FDA’s satisfaction, the FDA may initiate additional regulatory action without further notice. Any adverse regulatory action, depending on its magnitude, may restrict us from effectively manufacturing, marketing and selling our products and could have a material adverse effect on our business, financial condition and results of operations.Integration Activities
Revenues of products manufactured in the TEI Boston facility for the three months ended March 31, 2023 were approximately 4.4% of consolidated revenues.

OPTIMIZATION AND INTEGRATION ACTIVITIES
As a result of our ongoing acquisition strategy and significant growth in recent years, we have undertaken cost-saving initiatives to consolidate manufacturing operations, distribution facilities and transfer activities, eliminate duplicative positions, realign various sales and marketing activities, and expand and upgrade production capacity for our regenerative technology products. These efforts are expected to continue and while we expect a positive impact from ongoing restructuring, integration, and manufacturing transfer and expansion activities, such results remain uncertain. In support of our continued focus on product margins during 2022, we closed a manufacturing facility located in France and transferred production to our existing Switzerland facility. In 2022, we outsourced certain transactional back-office finance and customer service activities to enhance customer quality, build scale for future growth, and capture cost efficiencies.
RESULTS OF OPERATIONS
Executive Summary
Net incomeloss for the three months ended March 31, 20232024 was $3.3 million, or $0.04 per diluted share, as compared to net income of $24.2 million or $0.29 per diluted share as compared to $32.9 million or $0.39 per diluted share for the three months ended March 31, 2022.2023. The decrease in net income for the three months ended March 31, 2023,2024, was primarily driven by impacts from the SIA acquisition, including additional amortization, researchhigher manufacturing costs and development, and other costs.impairment charges of $7.1 million, primarily related to our Boston facility.
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Special Charges
Income before taxes includes the following special charges:
Three Months Ended March 31,
Three Months Ended March 31,
Three Months Ended March 31,
Three Months Ended March 31,
Dollars in thousandsDollars in thousands20232022Dollars in thousands20242023
Acquisition, divestiture and integration-related chargesAcquisition, divestiture and integration-related charges$8,776 $574 
Structural optimization chargesStructural optimization charges4,335 6,320 
EU medical device regulationEU medical device regulation11,404 9,513 
Boston recall expenses(1)
TotalTotal$24,515 $16,407 
(1) This primarily includes idle capacity charges and inventory write offs.
(1) This primarily includes idle capacity charges and inventory write offs.
The items reported above are reflected in the condensed consolidated statements of operations as follows:
Three Months Ended March 31,
Three Months Ended March 31,
Three Months Ended March 31,
Three Months Ended March 31,
Dollars in thousandsDollars in thousands20232022Dollars in thousands20242023
Cost of goods soldCost of goods sold$6,066 $4,530 
Research and developmentResearch and development4,218 4,267 
Selling, general and administrativeSelling, general and administrative14,730 8,902 
Other incomeOther income(499)(1,292)
Other income
Other income
Total Total$24,515 $16,407 
We typically define special charges as items for which the amounts and/or timing of such expenses may vary significantly from period to period, depending upon our acquisition, divestiture, integration and restructuring activities, and for which the amounts are non-cash in nature, and for which the amounts are not expected to recur at the same magnitude. We believe that given our ongoing strategy of seeking acquisitions, our continuing focus on rationalizing our existing manufacturing and distribution infrastructure and our continuing review of various product lines in relation to our current business strategy, some of the special charges discussed above could recur with similar materiality in the future.
We believe that the separate identification of these special charges provides important supplemental information to investors regarding financial and business trends relating to our financial condition and results of operations. Investors may find this information useful in assessing the comparability of our operating performance from period to period, against the business model objectives that management has established, and against other companies in our industry. We provide this information to investors so that they can analyze our operating results in the same way that management does and to use this information in their assessment of our core business and valuation of Integra.the Company.
Revenues and Gross Margin
The Company'sCompany’s revenues and gross margin on product revenues were as follows:
Three Months Ended March 31,Three Months Ended March 31,
Dollars in thousandsDollars in thousands20232022Dollars in thousands20242023
Segment Net SalesSegment Net Sales
Codman Specialty Surgical
Codman Specialty Surgical
Codman Specialty SurgicalCodman Specialty Surgical$248,136$247,308$256,434$248,136
Tissue TechnologiesTissue Technologies132,710129,330Tissue Technologies112,438132,710
Total revenuesTotal revenues$380,846$376,638Total revenues$368,872380,846
Cost of goods soldCost of goods sold147,975142,569Cost of goods sold162,038147,975
Gross margin on total revenuesGross margin on total revenues$232,871$234,069Gross margin on total revenues$206,834$232,871
Gross margin as a percentage of total revenuesGross margin as a percentage of total revenues61.1 %62.1 %Gross margin as a percentage of total revenues56.1 %61.1 %
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Three Months Ended March 31, 20232024 as Compared to Three Months Ended March 31, 20222023
Revenues
For the three months ended March 31, 2023,2024, total revenues increaseddecreased by $4.2$12.0 million to $380.8$368.9 million from $376.6$380.8 million for the same period in 2022,2023. This decrease was primarily driven by the impact of the Boston recall of $15.2 million. The decrease was also inclusive of aan unfavorable foreign currency impact of $7.0$2.4 million on revenues, as well as a $4.5 million decrease that impacts both domestic and international revenues related to the divestiture of the TWC business. This also includes an increase of $1.8 million related to the SIA acquisition.revenues. Excluding the impacts of these items, domestic revenues decreased by $1.3 million, or 0.5% compared to the same period in the prior year. International revenues increased by $6.8$8.7 million or 2.6%8.1% as compared to the prior year period. International revenues increased by $7.1 million or 6.5% as compared to the prior period. The increase in domestic revenues was primarily driven by strong sales in our TT segment. The increase in international revenues was primarily driven by Advanced Energy.
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increases in our APAC region, including China and Taiwan.
In the CSS segment, revenues were $248.1$256.4 million which was an increase of $0.8$8.3 million, or 0.3%3.3% as compared to the prior-year period, inclusive of a $6.4 $2.4 million unfavorable foreign currency impact on revenue. Excluding the impact of foreign exchange, the Neurosurgery portfolio grew low singlemid-single digits primarily due to increased sales in Advanced Energy. SalesNeuro Monitoring and CSF Management.
In the TT segment, revenues were $112.4 million which was a decrease of $20.3 million, or 15.3% from the prior-year period. This decrease is primarily driven by the impact of the Boston recall of $15.2 million decline in our instruments portfolio increased mid-single digits revenue. Excluding the impact of these items, the TT segment showed a decrease in sales as compared to the same period in the prior year.
In the TT segment, revenues were $132.7 million which was an increase of $3.4 million, or 2.6% from the prior-year period, inclusive of a $0.6 million unfavorable foreign currency impact on revenue, as well as a $4.5 million decrease that impacts both domesticyear, primarily attributable to Integra Skin MediHoney® and international revenues related to the divestiture of the TWC business. This also includes an increase of $1.8 million related to the SIA acquisition. Excluding the impact of these items, our sales increased mid single digits, driven by strong customer demand and increased burn cases.MicroMatrix®
Gross Margin
Gross margin was $232.9$206.8 million for the three months ended March 31, 2023,2024, a decrease of $1.2$26.0 million from $234.1$232.9 million for the same period in 2022.2023. Gross margin as a percentage of revenues was 61.1%56.1% for the three months ended March 31, 20232024 and 62.1%61.1% for the same period in 2022.2023. ThisThe decrease in gross margin is a result of unfavorable product mix and an increase inpercentage was primarily associated with higher costs related to idle capacity at our Boston facility, as well as additional manufacturing costs.expenses across our manufacturing sites.
Operating ExpensesExpenses
The following is a summary of operating expenses as a percent of total revenues:
Three Months Ended March 31, Three Months Ended March 31,
20232022 20242023
Research and developmentResearch and development7.0 %6.4 %Research and development7.3 %7.0 %
Selling, general and administrativeSelling, general and administrative43.8 %42.5 %Selling, general and administrative44.9 %43.8 %
Intangible asset amortizationIntangible asset amortization0.8 %1.0 %Intangible asset amortization2.7 %0.8 %
Total operating expensesTotal operating expenses51.6 %49.9 %Total operating expenses54.9 %51.6 %
Total operating expenses, which consist of research and development, selling, general and administrative, and amortization expenses, increased by $8.6$6.4 million, or 4.6%3.3% to $196.5$202.9 million in the three months ended March 31, 2023,2024, compared to $187.9$196.5 million in the same period in 2022. The increase in operating expenses compared to the prior year is primarily a result of the SIA acquisition combined with increases in selling costs associated with higher revenue.2023, mainly driven by intangible amortization.
Research and Development
Research and development expenses for the three months ended March 31, 20232024 increased by $2.6$0.2 million as compared to the same period in the prior year. This increase in spending resulted from additional spending related to the SIA acquisition, new product development and clinical studies.
Selling, General and Administrative
Selling, general and administrative costs for the three months ended March 31, 2023 increased2024 decreased by $6.7$0.9 million as compared to the same period in the prior year driven primarily due to increased selling costs associated with SIA acquisition and costs associated with consulting activities.year.
Intangible Asset Amortization
Amortization expense (excluding amounts reported in cost of product revenues for technology-based intangible assets) for the three months ended March 31, 20232024 was $3.1$10.1 million compared to $3.9$3.1 million for the same period in the prior year. The increase is driven by the impairment of customer relationship intangible related to our Boston facility.
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Non-Operating Income and Expenses
The following is a summary of non-operating income and expenses:
Three Months Ended March 31, Three Months Ended March 31,
Dollars in thousandsDollars in thousands20232022Dollars in thousands20242023
Interest incomeInterest income$4,107 $1,377 
Interest expenseInterest expense(12,100)(11,655)
Other income, netOther income, net1,389 3,429 
Other income, net
Other income, net
Total non-operating income and expenseTotal non-operating income and expense$(6,604)$(6,849)
Interest Income
Interest income for the three months ended March 31, 20232024 increased by $2.7$0.9 million as compared to the same period in the prior year primarily due to higher interest rates.
Interest Expense
Interest expense for the three months ended March 31, 2023 decreased2024 increased by $0.4$1.5 million as compared to the same period in the prior year.year primarily due incremental borrowing and higher interest rates.
Other Income, net
Other income, net for the three months ended March 31, 20232024 decreased by $2.0 million compared to the same period in the prior year. The decrease is primarily driven by lower Transition Service Agreement ("TSA"(“TSA”) income from the sale of our Extremity orthopedics business, offset by additional TSA income from the sale of our TWC business.divestitures.
Income Taxes
Three Months Ended March 31, Three Months Ended March 31,
Dollars in thousandsDollars in thousands20232022Dollars in thousands20242023
Income before income taxesIncome before income taxes$29,778 $39,315 
Income tax (benefit) expenseIncome tax (benefit) expense5,552 6,414 
Effective tax rateEffective tax rate18.6 %16.3 %Effective tax rate37.3 %18.6 %
Our effective income tax rates for the three months ended March 31, 2024 and 2023 were 37.3% and 2022 were 18.6% and 16.3%, respectively.
For the three months ended March 31, 2023,2024, the primary driverdrivers of the higher tax rate relates to a reduction of excess tax benefits$1.5 million expense due to a shortfall from stock compensation.based compensation, offset by a tax benefit for the intangible asset impairment, as compared to previous year. The Company does not have tax basis in the impaired intangible asset and has treated the tax impact as a discrete event in this quarter.
The effective tax rate may vary from period to period depending on, among other factors, the geographic and business mix of taxable earnings and losses, tax planning and settlements with various taxing authorities. We consider these factors and others, including the Company'sCompany’s history of generating taxable earnings, in assessing our ability to realize tax assets on a quarterly basis.
Additionally, changes to income tax laws and regulations, in any of the tax jurisdictions in which we operate,the Company operates, could impact the effective tax rate. Various governments, both U.S. and non-U.S., are increasingly focused on tax reform and revenue-raising legislation. The current U.S. administration has proposed tax reform which, if enacted, may increase the Company’s U.S. federal income tax liability. Further, legislation in foreign jurisdictions may be enacted, in response to the base erosion and profit-shifting project begun by the Organization for Economic Cooperation and Development ("OECD"(“OECD”). Such changes in the U.S. and non-U.S. jurisdictions could have an adverse effect on the Company's effective tax rate.
The OECD recently finalized major reform of the international tax system with respectreleased model rules related to implementing a new 15% global minimum tax rate.regime (“Pillar 2”). Several of the jurisdictions in which we operate have already adopted some form of the model rules, which could impact the amount of taxes that the Company pays during 2024 and future taxable periods. The rules are complex and provide for delays of implementing the tax during the early transition years, if certain conditions are met. At this time, the Company is projecting an immaterial amount related to Pillar 2 tax liability for the 2024 year. The Company will continue to analyze the new Pillar 2 laws and any related guidance to determine potential impacts. Such changes in U.S. and non-U.S. jurisdictions could have an adverse effect on the Company’s effective tax rate.
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As discussed previously, the Company recorded a total impairment charge of $7.1 million in intangible asset amortization during the first quarter of 2024. The Company does not have tax basis in the impaired customer relationship, therefore the charge resulted in a $1.6 million reduction of the Company’s deferred tax liability related to such intangible.
While it is often difficult to predict the outcome or the timing of the resolution of a particular matter with the various federal, state, and foreign tax authorities, we believe that our reserves reflect the most probable outcome of known tax contingencies. Settlement of a particular issue would usually require the use of cash. A favorable resolution would be recognized as a reduction to our annual effective tax rate in the year of resolution. OurThe Company’s tax reserves are presented in the balance sheet within other liabilities, except for amounts relating to items that we expect to pay in the coming year, which would be classified as current income taxes payable.
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GEOGRAPHIC PRODUCT REVENUES AND OPERATIONS
We attribute revenues to geographic areas based on the location of the customer. Total revenue by major geographic area consisted of the following:
Three Months Ended March 31,
Three Months Ended March 31,
Three Months Ended March 31,
Three Months Ended March 31,
Dollars in thousandsDollars in thousands20232022Dollars in thousands20242023
United StatesUnited States$271,002 $263,351 
EuropeEurope41,064 43,744 
Asia PacificAsia Pacific50,473 47,717 
Rest of WorldRest of World18,307 21,826 
Total RevenuesTotal Revenues$380,846 $376,638 
We generate significant revenues outside the U.S., a portion of which are U.S. dollar-denominated transactions conducted with customers that generate revenue in currencies other than the U.S. dollar. As a result, currency fluctuations between the U.S. dollar and the currencies in which those customers do business could have an impact on the demand for our products in foreign countries. Local economic conditions, regulatory compliance or political considerations, the effectiveness of our sales representatives and distributors, local competition and changes in local medical practice all may combine to affect our sales into markets outside the U.S.
Domestic revenues increaseddecreased by $7.7$14.8 million for the three months ended March 31, 20232024 compared to the same period last year. European sales decreasedincreased by $2.7$0.5 million for the three months ended March 31, 20232024 compared to the same period last year. Sales to customers in Asia Pacific increaseddecreased by $2.8$0.9 million for the three months ended March 31, 2023. The2024. Sales to customers in the the Rest of World for the three months ended March 31, 2023 decreased2024 increased by $3.5$3.2 million compared to the same period last year.year. The international revenues were impacted by $7.0$2.4 million of unfavorable foreign exchange impact, with the larger impact in Europe.Asia. The increasedecrease in global revenues inclusive of a $7.0 million unfavorable foreign exchange impact on revenue, is aprimarily the result of strong sales in our TT divisionthe Boston recall which affected both domestic and our international businesses. Sales in Japan, China, Europe, Canada and our indirect markets continue to drive international growth.markets.
LIQUIDITY AND CAPITAL RESOURCES
Working Capital
The Company'sCompany’s working capital as of March 31, 20232024 and December 31, 20222023 was $747.2$1,113.3 million and $840.6$751.1 million, respectively. Working capital consists of total current assets less total current liabilities as presented in the consolidated balance sheets.
Cash and Marketable Securities
The Company had cash and cash equivalents totaling approximately $307.4$591.9 million and $456.7$276.4 million at March 31, 20232024 and December 31, 20222023 respectively, which are valued based on Level 1 measurements in the fair value hierarchy. At March 31, 2023,2024, our non-U.S. subsidiaries held approximately $242.2$210.6 million of cash and cash equivalents that are available for use outside the U.S. The Company asserts that it has the ability and intends to indefinitely reinvest the undistributed earnings from its foreign operations unless there is no material tax cost to remit the earnings into the U.S..U.S.
Short Term Investments
The Company had short term investments, primarily consisting of time deposits, totaling approximately $71.2 million at March 31, 2024 compared to $32.7 million at December 31, 2023.

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Cash Flows
Three Months Ended March 31, Three Months Ended March 31,
Dollars in thousandsDollars in thousands20232022Dollars in thousands20242023
Net cash provided by operating activitiesNet cash provided by operating activities$26,156 $44,344 
Net cash used in investing activitiesNet cash used in investing activities(13,704)(14,067)
Net cash used in financing activities(162,683)(133,465)
Net cash provided by (used in) financing activities
Effect of exchange rate fluctuations on cashEffect of exchange rate fluctuations on cash937 (3,168)
Cash Flows Provided by Operating Activities
Operating cash flows for the three months ended March 31, 20232024 decreased by $18.2$10.4 million compared to the same period in 2022. 2023. Within operating cash flows, nNetet income after removing theless non-cash adjustments decreased for the three months ended March 31, 20232024 by approximately $5.3$29.7 million as compared to the same period in 20222023 primarily due to lowhigher product costs ander revenues attributable to the Boston recall, as well as additional manufacturing expenses related to support for key growth initiatives in research and development, selling and marketing areas.across our manufacturing sites.
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The changes in assets and liabilities in for the first quarter of 2023,three months ended March 31, 2024, net of business acquisitions, decreased cash flows by $42.6$23.4 million, mainly attributable to increases in inventory, to support increased sales and decreases in accrued expenses and other current liabilities due to increased payments processed in the quarter.and accounts receivable.
The changes in assets and liabilities infor the first quarter of 2022,three months ended March 31, 2023, net of business acquisitions, decreased cash flows by $29.842.6 million, primarily due to increases in inventory to support increased sales and decreases in accounts payable, accrued expenses and other current liabilities due to increased payments processed in the quarter.inventory.
Cash Flows Used in Investing Activities
DuringUses of cash from investing activities for the three months ended March 31, 2024 related to $38.5 million related to short term investments, and $15.5 million paid for capital expenditures to support operations improvement initiatives at a number of our manufacturing facilities and other information technology investments.
There were no sources of cash from investing activities during the three months ended March 31, 2024.
Uses of cash from investing activities during the three months ended March 31, 2023 we paidrelated to $13.7 million paid for capital expenditures to support operations improvement initiatives at a number of our manufacturing facilities and other information technology investments.
DuringThere were no sources of cash from investing activities during the three months ended March 31, 2022, we paid $9.3 million for capital expenditures to support operations improvement initiatives at a number of our manufacturing facilities and other information technology investments as well as the final $4.7 million payment related to the final developmental milestone for Rebound Therapeutics Corporation.2023.
Cash Flows Provided by or Used in Financing Activities
Uses of cash from financing activities in the three months ended March 31, 2024 related to the repayments of $15.1 million under our Senior Credit Facility and Securitization Facility. In addition, the Company had $3.1 million in cash taxes paid for net equity settlements.
Sources of cash from financing activities for the three months ended March 31, 2024 were $370.5 million proceeds from borrowings of long-term indebtedness and $6.4 million proceeds from the exercise of stock options.
Uses of cash from financing activities in the three months ended March 31, 2023 related to the repurchase of treasury stock of $150.0 million under the 2023 accelerated share repurchase agreement,agreements, repayments of $12.4 million under our Senior Credit Facility and Securitization Facility. We alsoIn addition, we had $7.6 million in payment ofattributable to debt issuance costs. In addition, the Company hadcosts, as well as $5.2 million in cash taxes paid for net equity settlements.
Sources of cash from financing activities for the three months ended March 31, 2023 were $10.2 million borrowing under our Senior Credit Facility and Securitization Facility and $2.3 million proceeds from the exercise of stock options.
Uses of cash from financing activities in the three months ended March 31, 2022 related to the repurchase of treasury stock of $125.0 million under the 2022 accelerated share repurchase agreement, repayments of $11.8 million under our Senior Credit Facility and Securitization Facility. In addition, we had $9.2 million in cash taxes paid for net equity settlements.
Sources of cash from financing activities for the three months ended March 31, 2022 were $11.3 million borrowing under our Senior Credit Facility and Securitization Facility and $1.2 million proceeds from the exercise of stock options.
Amended and Restated Senior Credit Agreement, Convertible Senior Notes, Securitization and Related Hedging Activities
See Note 6.6. Debt, to the Notes to Unaudited Condensed Consolidated Financial Statements (Part I, Item 1 of this Quarterly Report) for a discussion of our Amended and Restated Senior Credit Agreement, the 2025 Notes and Securitization Facility and Note 7, Derivative Instruments, to the Notes to Unaudited Condensed Consolidated Financial Statements (Part I, Item 1 of this Quarterly Report) for discussion of our hedging activities. We are forecasting that sales and earnings for the next twelve months will be sufficient to remain in compliance with our financial covenants under the terms
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Share Repurchase Plan
On January 26, 2023, we entered into ("the 2023 ASR") and received 2.1 million shares of our common stock at inception of the 2023 ASR, which represented approximately 80% of the expected total shares under the 2023 ASR. The remaining repurchase transactions are expected to be completed in the second quarter of 2023.
On January 12, 2022, we entered into a $125.0 million accelerated share repurchase ("2022 ASR") and received 1.48 million shares of our common stock at inception of the 2022 ASR, which represented approximately 80% of the expected total shares under the 2022 ASR. On March 24, 2022, the early exercise provision under the 2022 ASR was exercised by 2022 ASR counterparty. Upon settlement of the 2022 ASR on March 24, 2022, we received an additional 0.46 million shares determined using the volume-weighted average price of our common stock during the term of the 2022 ASR.
See Note 11.11, Treasury Stock, to the Notes to Unaudited Condensed Consolidated Financial Statements (Part I, Item 1 of this Quarterly Report) for further details.details of our share repurchase programs.
Dividend Policy
We have not paid any cash dividends on our common stock since our formation. Our Senior Credit Facility limits the amount of dividends that we may pay. Any future determinations to pay cash dividends on our common stock will be at the discretion of the Board of Directors and will depend upon our financial condition, results of operations, cash flows and other factors deemed relevant by the Board.
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Directors.
Capital Resources
We believe that our cash and available borrowings under the Senior Credit Facility are sufficient to finance our operations and capital expenditures for the next 12 months and foreseeable future. Our future capital requirements will depend on many factors, including the growth of our business, the timing and introduction of new products and investments, strategic plans and acquisitions, among others. Additional sources of liquidity available to us include short term borrowings and the issuance of long term debt and equity securities.
Off-Balance Sheet Arrangements
We do not have any off–balance sheet financing arrangements during the three months ended March 31, 20232024 that have or are reasonably likely to have, a current or future effect on our financial condition, changes in financial condition, revenues or expenses, results of operations, liquidity, capital expenditures or capital resources that are material to our interests.
Contractual Obligations and Commitments
We will continue to have cash requirements to support seasonal working capital needs and capital expenditures, to pay interest, to service debt, and to fund acquisitions. As part of our ongoing operations, we enter into contractual arrangements that obligate us to make future cash payments.
Our primary obligations include principal and interest payments on the revolving portion and tTerm Loanerm loan component of the Senior Credit Facility, Securitization Facility and Convertible Securities.2025 Notes. See Note 6. Debt, to the Notes to Unaudited Condensed Consolidated Financial Statements (Part I, Item 1 of this Quarterly Report) for details. We also lease some of our manufacturing facilities and office buildings which have future minimum lease payments associated.payments. See Note 10. Leases and Related Party Leases, to the Notes to Unaudited Condensed Consolidated Financial Statements (Part I, Item 1 of this Quarterly Report) for a schedule of our future minimum lease payments. Amounts related to our other obligations, including employment agreements and purchase obligations were not material.
The Company has contingent consideration obligationobligations related to prior and current year acquisitions and future pension contribution obligations. See Note 9. Retirement Plans, and Note 16. Commitments and Contingencies, to the Notes to Unaudited Condensed Consolidated Financial Statements (Part I, Item 1 of this Quarterly Report) for details. The associated obligations are not fixed. We also have a liability for uncertain tax benefits including interest and penalties. We cannot make a reliable estimate of the period in which the uncertain tax benefits may be realized.

OTHER MATTERS
Critical Accounting Estimates
We based the discussion and analysis of our financial condition and results of operations upon our consolidated financial statements, which have been prepared in conformity with GAAP. The preparation of these financial statements requires us to make estimates and assumptions that affect the reported amount of assets and liabilities, the disclosure of contingent liabilities, and the reported amounts of revenues and expenses. The critical accounting estimates includeddiscussed in our Annual Report on Form 10-K for the fiscal year ended December 31, 2022 have2023 did not materially changed.change in the three months ended March 31, 2024.
Recently Issued Accounting Standards
Information regarding new accounting pronouncements is included in Note 1. Basis of Presentation, to the Notes to Unaudited Condensed Consolidated Financial Statements (Part I, Item 1 of this Quarterly Report), and is applicable to the current period’s unaudited condensed consolidated financial statements.
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ITEM 3. QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK
We are exposed to various market risks, including changes in foreign currency exchange rates and interest rates that could adversely affect our results of operations and financial condition. To manage the volatility relating to these typical business exposures, we may enter into various derivative transactions when appropriate. We do not hold or issue derivative instruments for trading or other speculative purposes.
Foreign Currency Exchange and Other Rate Risks
We operate on a global basis and are exposed to the risk that changes in foreign currency exchange rates could adversely affect our financial condition, results of operations and cash flows. We are primarily exposed to foreign currency exchange rate risk with respect to transactions and net assets denominated in Euros, British pounds, Swiss francs, Canadian dollars, Japanese yen, Mexican pesos, Brazilian reais, Australian dollars, and Chinese yuan. We manage the foreign currency exposure centrally, on a combined basis, which allows us to net exposures and to take advantage of any natural offsets. To mitigate the impact of currency fluctuations on transactions denominated in nonfunctional currencies, we periodically enter into derivative financial instruments in the form of foreign currency exchange forward contracts with major financial institutions. We temporarily record realized and unrealized gains and losses on these contracts that qualify as cash flow hedges in other comprehensive income, and then recognize them in other income or expense when the hedged item affects net earnings.
From time to time, we enter into foreign currency forward exchange contracts to manage currency exposures for transactions denominated in a currency other than an entity’s functional currency. As a result, the impact of foreign currency gains/losses recognized in earnings are partially offset by gains/losses on the related foreign currency forward exchange contracts in the same reporting period. Refer to Note 7. Derivative Instruments, to Notes to Unaudited Condensed Consolidated Financial Statements (Part I, Item 1 of this Quarterly Report) for further information.
We maintain written policies and procedures governing our risk management activities. With respect to derivatives, changes in hedged items are generally expected to be completely offset by changes in the fair value of hedge instruments. Consequently, foreign currency exchange contracts would not subject us to material risk due to exchange rate movements, because gains and losses on these contracts offset gains and losses on the assets, liabilities or transactions being hedged.
The results of operations discussed herein have not been materially affected by inflation.
Interest Rate Risk
Cash and Cash Equivalents - We are exposed to the risk of interest rate fluctuations on the interest income earned on our cash and cash equivalents. A hypothetical 100 basis points movement in interest rates applicable to our cash and cash equivalents outstanding at March 31, 20232024 would impact interest income by approximately $3.1$5.9 million on an annual basis. We are subject to foreign currency exchange risk with respect to cash balances maintained in foreign currencies.
Debt - Our interest rate risk relates primarily to U.S. dollar SOFR-indexed borrowings. We use interest rate swap derivative instruments to manage our earnings and cash flow exposure to changes in interest rates. These interest rate swaps fix the interest rate on a portion of our expected SOFR-indexed floating-rate borrowings. These interest rate swaps were designated as cash flow hedges as of March 31, 2023.2024. The total notional amounts related to the Company’sCompany's interest rate swaps were $1.5 billion with $775.0 million effective as of March 31, 2023.2024. Based on our outstanding borrowings at March 31, 2023,2024, a 100 basis points change in interest rates would have impacted interest expense on the unhedged portion of the debt by $1.0$5.1 million on an annualized basis. See Note 7. Derivative Instruments, to the Notes to Unaudited Condensed Consolidated Financial Statements (Part I, Item 1 of this Quarterly Report) for further information regarding interest rate swaps.
ITEM 4. CONTROLS AND PROCEDURES
Evaluation of Disclosure Controls and Procedures
We maintain disclosure controls and procedures that are designed to provide reasonable assurance that information required to be disclosed in our Exchange Act reportreports is recorded, processed, summarized and reported within the time periods specified in the SEC’s rules and forms and that such information is accumulated and communicated to our management, including our principal executive officer and principal financial officer, as appropriate, to allow timely decisions regarding required disclosure. Disclosure controls and procedures, no matter how well designed and operated, can provide only reasonable assurance of achieving the desired control objectives, and management is required to apply its judgment in evaluating the cost-benefit relationship of possible controls and procedures. Management has designed our disclosure controls and procedures to provide reasonable assurance of achieving the desired control objectives.
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As required by Exchange Act Rule 13a-15(b), we have carried out an evaluation, under the supervision and with the participation of our management, including our principal executive officer and principal financial officer, of the effectiveness of the design and operation of our disclosure controls and procedures as of March 31, 2023.2024. Based upon this evaluation, our principal executive officer and principal financial officer concluded that our disclosure controls and procedures were effective as of March 31, 20232024 to provide such reasonable assurance.
Changes in Internal Control Over Financial Reporting
There were no changes in our internal control over financial reporting (as defined in Rule 13a-15(f) under the Exchange Act) that occurred during the quarter ended March 31, 20232024 that have materially affected, or are reasonably likely to materially affect, our internal control over financial reporting.
In response to business integration activities, we have and will continue to further align and streamline the design and operation of the financial control environment to be responsive to the changing business model.
PART II. OTHER INFORMATION
ITEM 1. LEGAL PROCEEDINGS
Information pertainingPlease refer to legal proceedings can be found in Note 16, CommitmentCommitments and Contingencies,, to the Notes to Unaudited Condensed Consolidated Financial Statements (Part I, Item 1 of this Quarterly Report). for further details on current legal proceedings.
ITEM 1A. RISK FACTORS
There have been no material changes in our risk factors included in our Annual Report on Form 10-K for the fiscal year ended December 31, 20222023 and subsequent periodic reports filed with the Securities and Exchange Commission pursuant to the Securities Exchange Act of 1934, as amended (the "Exchange Act").Act.
ITEM 2. UNREGISTERED SALES OF EQUITY SECURITIES AND USE OF PROCEEDS
The following table provides information about purchases by us during the quarter ended March 31, 2023Recent Sale of equity securities that are registered by us pursuant to Section 12Unregistered Securities:
None.
Purchase of the Exchange Act. Subject to applicable law, share repurchases may be made from time to time in open market transactions, privately negotiated transactions including accelerated share repurchase agreements, or pursuant to instruments and plans complying with Rule 10b5-1 under the Exchange Act, among other types of transactions and arrangements.Equity Securities
Issuer purchases of equity securities
PeriodTotal number of shares purchased by monthAverage price paid per shareTotal number of shares purchased by month as part of publicly announced repurchase programsApproximate dollar value of shares that may yet be purchased under the plans or program
01/01/23 - 01/31/232,111,189 $56.68 2,111,189 30,000,000 
02/01/23 - 02/28/23— — — — 
03/01/23 - 03/31/23— — — — 
2,111,189 $56.68 2,111,189 30,000,000 
On January 26, 2023, the Company entered into the 2023 ASR and received 2.1 million shares of our common stock at inception of the 2023 ASR, which represented approximately 80% of the expected total shares under the 2023 ASR. The remaining repurchase transactions are expected to be completed in the second quarter of 2023.
See Note 11, Treasury Stock, to the Notes to Consolidated Financial Statements (Part I, Item 1 of this Quarterly Report) for additional information regarding our share repurchase program and the 2023 ASR.None.
ITEM 3. DEFAULTS UPON SENIOR SECURITIES
Not applicable.
ITEM 4. MINE SAFETY DISCLOSURES
Not applicable.
ITEM 5. OTHER INFORMATION
Not applicable.Rule 10b5-1 Trading Plans
During the quarter ended March 31, 2024, none of the Company’s directors or officers adopted or terminated any contract, instruction or written plan for the purchase or sale of Company securities that was intended to satisfy the affirmative defense conditions of Rule 10b5-1(c) or any “non-Rule 10b5-1 trading arrangement.”
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ITEM 6. EXHIBITS
Exhibits
3.1(a)
3.1(b)
3.1(c)
3.1(d)
3.2
3.3
10.110.1*
10.210.2*+
10.3(a)
10.3(b)
10.3(c)
10.3(d)
10.3(e)
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*10.4
*31.131.1+ 
*31.231.2+ 
*32.132.1+ 
*32.232.2+ 
*†101.INS101.INS+# XBRL Instance Document - the instance document does not appear in the Interactive Data File because its XBRL tags are embedded within the Inline XBRL document.
*†101.SCH101.SCH+# XBRL Taxonomy Extension Schema Document
*†101.CAL101.CAL+# XBRL Taxonomy Extension Calculation Linkbase Document
*†101.DEF101.DEF+# XBRL Definition Linkbase Document
*†101.LAB101.LAB+# XBRL Taxonomy Extension Labels Linkbase Document
*†101.PRE101.PRE+# XBRL Taxonomy Extension Presentation Linkbase Document
104Cover Page Interactive Data File (formatted as Inline XBRL and contained in Exhibit 101)
 
*Filed herewith
#Indicates a management contract or compensatory plan or arrangement.
+Indicates this document is filed as an exhibit herewith.
#The financial information of Integra LifeSciences Holdings Corporation Quarterly Report on Form 10-Q for the quarter ended March 31, 20232024 filed on April 26, 202305/06/2024 formatted in XBRL (Extensible Business Reporting Language): (i) the Condensed Consolidated Statements of Operations and Comprehensive Income, (ii) the Condensed Consolidated Balance Sheets, (iii) Parenthetical Data to the Condensed Consolidated Balance Sheets, (iv) the Condensed Consolidated Statements of Cash Flows, and (v) Notes to Condensed Consolidated Financial Statements, is furnished electronically herewith.
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SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized.
 
 INTEGRA LIFESCIENCES HOLDINGS CORPORATION
Date:April 26, 2023May 6, 2024/s/ Jan De Witte
 Jan De Witte
 President and Chief Executive Officer
(Principal Executive Officer)
Date:April 26, 2023May 6, 2024/s/ Lea Knight
Lea Knight
Executive Vice President and Chief Financial Officer
(Principal Financial Officer)
Date:May 6, 2024/s/ Jeffrey A. Mosebrook
 Jeffrey A. Mosebrook
 Senior Vice President, Finance
(Principal Financial Officer and Principal Accounting Officer)

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