Hologic (HOLX) 10-Q 2013 Q1 Quarterly report

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

FORM 10-Q

(Mark One)

x QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the quarterly period ended December 29, 2012

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 Number: 0-18281

Hologic, Inc.

(Exact name of registrant as specified in its charter)

Delaware	04-2902449
(State of incorporation)	(I.R.S. Employer Identification No.)
35 Crosby Drive, Bedford, Massachusetts	01730
(Address of principal executive offices)	(Zip Code)

(781) 999-7300

(Registrant’s telephone number, including area code)

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  x    No  ¨

Indicate by check mark whether the registrant has submitted electronically and posted on its corporate Web site, if any, every Interactive Data File required to be submitted and posted 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 and post such files).    Yes  x    No  ¨

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, or a smaller reporting company. See the definitions of “large accelerated filer,” “accelerated filer” and “smaller reporting company” in Rule 12b-2 of the Exchange Act. (Check One):

Large accelerated filer	x	Accelerated filer	¨
Non-accelerated filer	¨  (Do not check if a smaller reporting company)	Smaller reporting company	¨

Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act.)    Yes  ¨    No  x

As of January 30, 2013, 267,696,863 shares of the registrant’s Common Stock, $0.01 par value, were outstanding.

HOLOGIC, INC.

INDEX

	Page
PART I – FINANCIAL INFORMATION
Item 1. Financial Statements (unaudited)
Consolidated Statements of Income for the Three Months Ended December 29, 2012 and December  24, 2011		3
Consolidated Statements of Comprehensive Income for the Three Months Ended December  29, 2012 and December 24, 2011		4
Consolidated Balance Sheets as of December 29, 2012 and September 29, 2012		5
Consolidated Statements of Cash Flows for the Three Months Ended December 29, 2012 and December  24, 2011		6
Notes to Consolidated Financial Statements		7
Item 2. Management’s Discussion and Analysis of Financial Condition and Results of Operations		30
Item 3. Quantitative and Qualitative Disclosures About Market Risk		43
Item 4. Controls and Procedures		44
PART II – OTHER INFORMATION		45
SIGNATURES		47
EXHIBITS

2

PART I – FINANCIAL INFORMATION

Item 1. Financial Statements (unaudited)

HOLOGIC, INC.

CONSOLIDATED STATEMENTS OF INCOME

(Unaudited)

(In thousands, except per share data)

	Three Months Ended
	December 29, 2012			December 24, 2011
Revenues:
Product sales	$	535,202		$	392,096
Service and other revenues		96,160			80,615
		631,362			472,711
Costs and expenses:
Cost of product sales		223,493			131,944
Cost of product sales – amortization of intangible assets		75,287			46,171
Cost of service and other revenues		50,909			45,226
Research and development		51,509			28,342
Selling and marketing		94,443			77,460
General and administrative		54,391			46,495
Amortization of intangible assets		28,526			14,842
Contingent consideration – compensation expense		29,486			10,441
Contingent consideration – fair value adjustments		10,040			5,122
Gain on sale of intellectual property, net		(53,884	)		—
Restructuring charges, net		3,933			(91	)
		568,133			405,952
Income from operations		63,229			66,759
Interest income		260			662
Interest expense		(72,081	)		(29,509	)
Other income, net		1,239			1,992
(Loss) income before income taxes		(7,353	)		39,904
(Benefit) provision for income taxes		(10,471	)		19,092
Net income	$	3,118		$	20,812
Net income per common share:
Basic	$	0.01		$	0.08
Diluted	$	0.01		$	0.08
Weighted average number of common shares outstanding:
Basic		266,344			262,717
Diluted		269,379			264,958

See accompanying notes.

3

HOLOGIC, INC.

CONSOLIDATED STATEMENTS OF COMPREHENSIVE INCOME

(Unaudited)

(In thousands)

	Three Months Ended
	December 29, 2012			December 24, 2011
Net income	$	3,118		$	20,812
Foreign currency translation adjustment		1,969			(358	)
Unrealized loss on available-for-sale security		(557	)		—
Other comprehensive income (loss)		1,412			(358	)
Comprehensive income	$	4,530		$	20,454

See accompanying notes.

4

HOLOGIC, INC.

CONSOLIDATED BALANCE SHEETS

(Unaudited)

(In thousands, except per share data)

	December 29, 2012			September 29, 2012
ASSETS
Current assets:
Cash and cash equivalents	$	718,471		$	560,430
Restricted cash		2,094			5,696
Accounts receivable, less reserves of $6,662 and $6,396, respectively		405,653			409,333
Inventories		345,309			367,191
Deferred income tax assets		—			11,715
Prepaid income taxes		51,307			69,845
Prepaid expenses and other current assets		45,950			44,301
Other current assets – assets held-for-sale		91,452			94,503
Total current assets		1,660,236			1,563,014
Property, plant and equipment, net		504,071			507,998
Intangible assets, net		4,195,538			4,301,250
Goodwill		3,941,430			3,942,779
Other assets		167,280			162,067
Total assets	$	10,468,555		$	10,477,108
LIABILITIES AND STOCKHOLDERS’ EQUITY
Current liabilities:
Accounts payable	$	76,367		$	87,223
Accrued expenses		436,283			372,381
Deferred revenue		121,152			129,688
Current portion of long-term debt		798,937			64,435
Deferred income tax liabilities		111,611			—
Other current liabilities – assets held-for-sale		7,403			7,622
Total current liabilities		1,551,753			661,349
Long-term debt, net of current portion		4,237,085			4,971,179
Deferred income tax liabilities		1,576,472			1,771,585
Deferred service obligations – long-term		16,440			13,714
Other long-term liabilities		102,429			98,250
Commitments and contingencies (Note 6)
Stockholders’ equity:
Preferred stock, $0.01 par value – 1,623 shares authorized; 0 shares issued		—			—
Common stock, $0.01 par value – 750,000 shares authorized; 267,373 and 265,635 shares issued, respectively		2,674			2,656
Additional paid-in-capital		5,415,454			5,396,657
Accumulated deficit		(2,440,436	)		(2,443,554	)
Accumulated other comprehensive income		8,202			6,790
Treasury stock, at cost – 219 shares		(1,518	)		(1,518	)
Total stockholders’ equity		2,984,376			2,961,031
Total liabilities and stockholders’ equity	$	10,468,555		$	10,477,108

See accompanying notes.

5

HOLOGIC, INC.

CONSOLIDATED STATEMENTS OF CASH FLOWS

(Unaudited)

(In thousands)

	Three Months Ended
	December 29, 2012			December 24, 2011
OPERATING ACTIVITIES
Net income	$	3,118		$	20,812
Adjustments to reconcile net income to net cash provided by operating activities:
Depreciation		24,342			16,110
Amortization		103,813			61,013
Non-cash interest expense – amortization of debt discount and deferred financing costs		20,679			19,960
Stock-based compensation expense		12,066			8,657
Excess tax benefit related to equity awards		(2,185	)		(1,725	)
Deferred income taxes		(70,123	)		(13,106	)
Gain on sale of intellectual property, net		(53,884	)		—
Fair value adjustments to contingent consideration		10,040			5,122
Fair value write-up of inventory sold		29,876			—
Loss on disposal of property and equipment		906			373
Other		(1,149	)		(1,825	)
Changes in operating assets and liabilities:
Accounts receivable		6,903			(6,616	)
Inventories		(6,004	)		(11,474	)
Prepaid income taxes		18,538			340
Prepaid expenses and other assets		(1,177	)		(530	)
Accounts payable		(10,629	)		(499	)
Accrued expenses and other liabilities		76,138			11,306
Deferred revenue		(6,243	)		3,813
Net cash provided by operating activities		155,025			111,731
INVESTING ACTIVITIES
Payment of additional acquisition consideration		(16,808	)		(9,784	)
Proceeds from sale of business, net of cash transferred		1,488			—
Purchase of property and equipment		(11,233	)		(6,790	)
Increase in equipment under customer usage agreements		(11,214	)		(7,886	)
Purchase of insurance contracts		(4,000	)		—
Proceeds from sale of intellectual property		60,000			—
Purchase of cost method investments		(3,625	)		(150	)
Decrease in other assets		1,144			9
Net cash provided by (used in) investing activities		15,752			(24,601	)
FINANCING ACTIVITIES
Repayment of long-term debt		(16,250	)		—
Payment of contingent consideration		(3,408	)		(4,105	)
Net proceeds from issuance of common stock pursuant to employee stock plans		12,777			1,627
Excess tax benefit related to equity awards		2,185			1,725
Payment of employee restricted stock minimum tax withholdings		(7,885	)		(5,561	)
Net cash used in financing activities		(12,581	)		(6,314	)
Effect of exchange rate changes on cash and cash equivalents		(155	)		(66	)
Net increase in cash and cash equivalents		158,041			80,750
Cash and cash equivalents, beginning of period		560,430			712,332
Cash and cash equivalents, end of period	$	718,471		$	793,082

See accompanying notes.

6

HOLOGIC, INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS

(Unaudited)

(all tabular amounts in thousands except per share data)

(1) Basis of Presentation

The consolidated financial statements of Hologic, Inc. (the “Company”) presented herein have been prepared pursuant to the rules of the Securities and Exchange Commission for quarterly reports on Form 10-Q and do not include all of the information and disclosures required by U.S. generally accepted accounting principles. These financial statements should be read in conjunction with the consolidated financial statements and notes thereto for the year ended September 29, 2012, included in the Company’s Form 8-K filed with the Securities and Exchange Commission on January 28, 2013. The Form 8-K was filed to add a footnote to the consolidated financial statements for the requirement to provide financial information of the Company’s guarantors of its Senior Notes in connection with registering the Senior Notes on a Registration Statement on Form S-4 filed with the Securities and Exchange Commission on January 28, 2013. In the opinion of management, the financial statements and notes contain all adjustments (consisting of normal recurring accruals) considered necessary for a fair presentation of the Company’s financial position, results of operations and cash flows for the periods presented.

The consolidated financial statements include the accounts of the Company and its wholly owned subsidiaries. All intercompany transactions and balances have been eliminated in consolidation.

The preparation of financial statements in conformity with U.S. generally accepted accounting principles requires management to make significant estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of revenues and expenses during the reporting periods. Actual results could differ from management’s estimates if past experience or other assumptions do not turn out to be substantially accurate. Operating results for the three months ended December 29, 2012 are not necessarily indicative of the results to be expected for any other interim period or the entire fiscal year ending September 28, 2013.

Subsequent Events Consideration

The Company considers events or transactions that occur after the balance sheet date but prior to the issuance of the financial statements to provide additional evidence for certain estimates or to identify matters that require additional disclosure. Subsequent events have been evaluated as required. There were no material recognized subsequent events recorded in the unaudited consolidated financial statements as of and for the three months ended December 29, 2012.

(2) Fair Value Measurements

Assets/Liabilities Measured and Recorded at Fair Value on a Recurring Basis

As of December 29, 2012 and September 29, 2012, the Company’s financial assets that are re-measured at fair value on a recurring basis included $0.3 million in money market mutual funds in both periods that are classified as cash and cash equivalents in the Consolidated Balance Sheets. Money market funds are classified within Level 1 of the fair value hierarchy and are valued using quoted market prices for identical assets. As a result of its Gen-Probe acquisition, the Company has an equity investment in a publicly-traded company and mutual funds, both of which are valued using quoted market prices, representing Level 1 assets. The Company has a payment obligation to the participants under its Nonqualified Deferred Compensation Plan (“DCP”) and the deferred compensation plan assumed in the Gen-Probe acquisition. This aggregate liability is recorded at fair value based on the underlying value of certain hypothetical investments under the DCP and actual investments under the plan assumed from Gen-Probe as designated by each participant for their benefit. Since the value of the deferred compensation plan obligations are based on market prices, the liability is classified within Level 1. In addition, the Company has contingent consideration liabilities related to its acquisitions that are recorded at fair value. The fair values of these liabilities are based on Level 3 inputs and are discussed in Notes 3 and 6(a).

7

Assets and liabilities measured and recorded at fair value on a recurring basis consisted of the following at December 29, 2012:

			Fair Value at Reporting Date Using
	Balance as of December 29, 2012		Quoted Prices in Active Market for Identical Assets (Level  1)		Significant Other Observable Inputs (Level 2)		Significant Unobservable Inputs (Level 3)
Assets:
Money market funds	$	315	$	315	$	—	$	—
Marketable securities:
Equity security		5,472		5,472		—		—
Mutual funds		6,618		6,618		—		—
Total	$	12,405	$	12,405	$	—	$	—
Liabilities:
Deferred compensation liabilities	$	34,852	$	34,852	$	—	$	—
Contingent consideration		93,000		—		—		93,000
Total	$	127,852	$	34,852	$	—	$	93,000

Changes in the fair value of recurring fair value measurements, which solely consisted of contingent consideration liabilities, using significant unobservable inputs (Level 3) were as follows:

	Three Months Ended
	December 29, 2012			December 24, 2011
Balance at beginning of period	$	86,368		$	103,790
Fair value adjustments		10,040			5,122
Payments made		(3,408	)		(4,105	)
Balance at end of period	$	93,000		$	104,807

Assets Measured and Recorded at Fair Value on a Nonrecurring Basis

The Company remeasures the fair value of certain assets and liabilities upon the occurrence of certain events. Such assets are comprised of cost-method equity investments and long-lived assets, including property, plant and equipment, intangible assets and goodwill.

The Company holds certain cost-method equity investments in non-publicly traded securities aggregating $19.6 million and $16.0 million at December 29, 2012 and September 29, 2012, respectively, which are included in other long-term assets on the Company’s Consolidated Balance Sheets. These investments are generally carried at cost. As the inputs utilized for the Company’s periodic impairment assessment are not based on observable market data, these cost method investments are classified within Level 3 of the fair value hierarchy. To determine the fair value of these investments, the Company uses all available financial information related to the entities, including information based on recent or pending third-party equity investments in these entities. In certain instances, a cost method investment’s fair value is not estimated as there are no identified events or changes in circumstances that may have a significant adverse effect on the fair value of the investment and to do so would be impractical.

Disclosure of Fair Value of Financial Instruments

The Company’s financial instruments mainly consist of cash and cash equivalents, accounts receivable, marketable securities, cost-method equity investments, insurance contracts, deferred compensation plan liabilities, accounts payable and debt obligations. The carrying amounts of the Company’s cash equivalents, accounts receivable and accounts payable approximate their fair value due to the short-term nature of these instruments. The carrying amount of the insurance contracts are recorded at the cash surrender value, as required by U.S. generally accepted accounting principles, which approximates fair value, and the related DCP liability is recorded at fair value. The Company believes the carrying amounts of its cost-method investments approximate fair value.

Amounts outstanding under the Company’s Credit Agreement of $2.48 billion aggregate principal are subject to variable rates of interest based on current market rates, and as such, the Company believes the carrying amount of these obligations approximates fair value. In addition, based on the recent issuance of its Senior Notes, the Company believes their carrying amount approximates fair value.

8

The fair value of the Company’s Convertible Notes is based on the trading prices of the respective notes at the dates noted and represents a Level 1 measurement. The Company had $1.57 billion and $1.56 billion of Convertible Notes recorded (See Note 5) as of December 29, 2012 and September 29, 2012, respectively. The aggregate principal amount of the Convertible Notes at both periods was $1.725 billion. The Company has three issues of Convertible Notes outstanding: 2007 Notes (principal of $775.0 million), 2010 Notes (principal of $450.0 million), and the 2012 Notes (principal of $500.0 million).

The estimated fair values of the Company’s Convertible Notes are as follows:

	December 29, 2012		September 29, 2012
2007 Notes	$	771,100	$	771,600
2010 Notes		504,700		505,600
2012 Notes		496,300		490,700
	$	1,772,100	$	1,767,900

(3) Business Combinations

Gen-Probe Incorporated

On August 1, 2012, the Company completed the acquisition of Gen-Probe and acquired all of the outstanding shares of Gen-Probe. Pursuant to the merger agreement, each share of common stock outstanding immediately prior to the effective time of the acquisition was cancelled and converted into the right to receive $82.75 in cash. In addition, all outstanding restricted shares, restricted stock units, performance shares, and those stock options granted prior to February 8, 2012 were cancelled and converted into the right to receive $82.75 per share in cash less the exercise price, as applicable. Stock options granted after February 8, 2012 were converted into stock options to acquire shares of Hologic common stock determined by the conversion formula defined in the merger agreement. The Company paid the Gen-Probe shareholders $3.8 billion and $169.0 million to equity award holders. The Company funded the acquisition using available cash and financing consisting of senior secured credit facilities and Senior Notes (see Note 5 for further discussion) resulting in aggregate proceeds of $3.48 billion, excluding financing fees to the underwriters. The Company incurred approximately $34.3 million of direct transaction costs, which were recorded within general and administrative expenses in fiscal 2012.

Gen-Probe, headquartered in San Diego, California, is a leader in molecular diagnostics products and services that are used primarily to diagnose human diseases and screen donated human blood. The Company expects this acquisition to enhance its molecular diagnostics franchise and to complement its existing portfolio of diagnostics products. Gen-Probe’s results of operations are reported within the Company’s Diagnostics reportable segment from the date of acquisition.

The purchase price consideration was as follows:

Cash paid	$	3,967,866
Deferred payment		1,655
Fair value of stock options exchanged		2,655
Total purchase price	$	3,972,176

The fair value of stock options exchanged, that were recorded as purchase price, represents the fair value of the Gen-Probe options converted into the Company’s stock options attributable to pre-combination services pursuant to ASC 805,Business Combinations (ASC 805). The remainder of the fair value of these stock options of $23.2 million will be recognized as stock-based compensation expense over the remaining vesting period, which is approximately 3.5 years. The Company estimated the fair value of the stock options using a binomial valuation model with the following weighted average assumptions: risk free rate of 0.41%, expected volatility of 39.9%, expected life of 3.6 years and dividend of 0.0%. The weighted average fair value of stock options granted is $7.07 per share.

9

The preliminary allocation of the purchase price presented below is based on estimates of the fair value of assets acquired and liabilities assumed as of August 1, 2012. The Company is continuing to obtain information to complete its valuation of intangible assets, as well as to determine the acquired assets and liabilities, including tax assets and liabilities. The components of the preliminary purchase price allocation are as follows:

Cash	$	205,463
Accounts receivable		80,301
Inventory		153,416
Property, plant and equipment		274,095
Other assets		191,868
Assets held-for-sale, net		87,465
Accounts payable		(19,671	)
Accrued expenses		(131,102	)
Other liabilities		(19,255	)
Identifiable intangible assets:
Developed technology		1,565,000
In-process research and development		227,000
Customer contract		585,000
Trade names		95,000
Deferred income taxes, net		(973,524	)
Goodwill		1,651,120
Purchase Price	$	3,972,176

The purchase price has been allocated to the acquired assets and liabilities based on management’s estimate of their fair values. During the first quarter of fiscal 2013, as the Company continues to complete its valuation procedures, it lowered the valuation of trade names by $2.0 million with an offsetting increase to goodwill. In addition, certain tax related adjustments were recorded.

Certain of Gen-Probe’s assets have been designated as assets held-for-sale and have been recorded at fair value less the estimated cost to sell such assets. These represent non-core assets to the Company’s business plan and are expected to be sold within one year of the acquisition. In the first quarter of fiscal 2013, the Company completed the sale of one of these asset groups for $2.2 million. On January 3, 2013, the Company entered into a definitive agreement to sell its LIFECODES business to Immucor for $85.0 million in cash, subject to adjustment, plus a contingent payment of an additional $10.0 million based on future revenue results. LIFECODES sells molecular and antibody-based assays in the markets of transplant diagnostics, specialty coagulation and transfusion medicine. The transaction is subject to customary closing conditions, including expiration of the applicable waiting periods under the Hart-Scott-Rodino Antitrust Improvements Act of 1976, as amended, and an international regulatory review and is expected to close in the first half of fiscal 2013. Assets and liabilities held for sale are reflected separately in the Company’s Consolidated Balance Sheet. The following represents the components of the asset groups classified as held-for-sale as of December 29, 2012:

Assets:
Cash	$	2,272
Accounts receivable		7,549
Inventory		14,469
Property and equipment		13,431
Other assets		1,851
Intangible assets and goodwill		51,880
Total assets held-for-sale	$	91,452
Liabilities:
Accrued liabilities		(7,403	)
Net assets held-for-sale	$	84,049

As part of the preliminary purchase price allocation, the Company has determined the identifiable intangible assets are developed technology, in-process research and development (“IPR&D”), customer contracts, and trade names.The fair value of the intangible assets has been estimated using the income approach and the cash flow projections were discounted using rates ranging from 10% to 12%. The cash flows are based on estimates used to price the transaction, and the discount rates applied were benchmarked with reference to the implied rate of return from the transaction model and the weighted average cost of capital.

The developed technology assets are comprised of know-how, patents and technologies embedded in Gen-Probe’s products and relate to currently marketed products and related instrument automation. In valuing the developed technology assets, consideration was only given to products that have received regulatory approval. The developed technology assets primarily comprise the significant product families used in diagnostic testing, and the majority of fair value relates to the APTIMA family of assays for testing of certain sexually transmitted diseases and microbial infectious diseases and the PROCLEIX family of assays for blood screening. The Company applied the Excess Earnings Method under the income approach to fair value the developed technology assets excluding the PROCLEIX technology asset. The Company applied the Relief-from-Royalty Method to fair value this asset.

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IPR&D projects relate to in-process projects that have not reached technological feasibility as of the acquisition date and have no alternative future use. The primary basis for determining technological feasibility of these projects is obtaining regulatory approval to market the underlying product, which primarily pertains to receiving approval to perform certain diagnostic testing on Gen-Probe’s instrumentation, such as the PANTHER and TIGRIS systems. The Company recorded $227.0 million of IPR&D related to 6 projects. One project, valued at $7.0 million, received FDA approval in October 2012, and another project, valued at $27.0 million, received FDA approval in January 2013. Amortization of these assets begins once FDA approval is received. The other projects are expected to be completed within the next 6 months to 42 months with a total cost of approximately $51 million to complete such projects. Given the uncertainties inherent with product development and commercial introduction, there can be no assurance that any of the Company’s product development efforts will be successful, completed on a timely basis or within budget, if at all. All of the IPR&D assets were valued using the multiple-period excess earnings method approach using a discount rate of 12.0%.

The customer contract intangible asset pertains to Gen-Probe’s relationship with Novartis, and the Company used the Excess Earnings Method to estimate the fair value of this asset. Trade names relate to the Gen-Probe corporate name and the primary product names, and the Company used the Relief-from-Royalty Method to estimate the fair value of this asset.

Developed technology, customer contract and trade names are being amortized on a straight-line basis over a weighted average period of 12.5 years, 13.0 years and 11.0 years, respectively.

The Company estimated the fair value of property, plant and equipment using a combination of the cost and market approaches, depending on the component. The Company applied the cost approach as the primary method in estimating the fair value of land and buildings. In total, the fair value adjustment to increase the carrying amount of property, plant and equipment was $107.9 million, of which $70.6 million related to land and buildings.

The excess of the purchase price over the estimated fair value of the tangible net assets and intangible assets acquired was recorded to goodwill. The factors contributing to the recognition of the amount of goodwill were based on several strategic and synergistic benefits that are expected to be realized from the Gen-Probe acquisition. These benefits include the expectation that the combined company’s complementary products in the molecular diagnostics market with Gen-Probe’s fully automated product franchise will significantly broaden the Company’s offering in women’s health and diagnostics. The combined company is expected to benefit from a broader global presence and with Hologic’s direct sales force and marketing in Europe and its investment in China distribution, the growth prospects of Gen-Probe’s products are expected to be enhanced significantly. The combined company anticipates significant cross-selling opportunities within the diagnostics market through Hologic’s larger channel coverage and physician sales team. None of the goodwill is expected to be deductible for income tax purposes.

The following unaudited pro forma information presents the combined financial results for the Company and Gen-Probe as if the acquisition of Gen-Probe had been completed as of the beginning of the fiscal year prior to the period of acquisition, September 26, 2010:

	Three Months Ended December 24, 2011
Revenue	$	630,844
Net loss	$	(10,195	)
Basic and diluted net loss per common share	$	(0.04	)

The unaudited pro forma information for the three months ended December 24, 2011 was calculated after applying the Company’s accounting policies and the impact of acquisition date fair value adjustments. These pro forma condensed consolidated financial results have been prepared for comparative purposes only and include certain adjustments to reflect pro forma results of operations as if the acquisition occurred on September 26, 2010, such as fair value adjustments to inventory, accounts receivable, and property, plant and equipment, increased expenses for restructuring charges and retention costs, increased interest expense on debt obtained to finance the transaction, lower investment income and increased amortization for the fair value of acquired intangible assets. The pro forma information does not reflect the effect of costs, other than restructuring and retention, or synergies that would have been expected to result from the integration of the acquisition. The pro forma information does not purport to be indicative of the results of operations that actually would have resulted had the combination occurred at the beginning of each period presented, or of future results of the consolidated entities.

(4) Restructuring Charges

In addition to monitoring the global macro-economic environment and impact on its businesses and products, the Company also evaluates its operations for opportunities to improve operational effectiveness and efficiency and to better align expenses with

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revenues. As a result of these assessments, the Company has undertaken various restructuring actions. These actions are described below. The following table displays charges taken related to restructuring actions in fiscal 2013 and 2012 and a rollforward of the charges to the accrued balances as of December 29, 2012.

Restructuring Charges	Abandonment of Adiana Product Line			Consolidation of Diagnostics Operations			Closure of Indianapolis Facility			Other Operating Cost Reductions			Total
Fiscal 2012 charges:
Non-cash impairment charge	$	16,316		$	585		$	—		$	—		$	16,901
Purchase orders and other contractual obligations		3,099			—			—			—			3,099
Workforce reductions		128			14,202			879			40			15,249
Facility closure costs		—			—			—			430			430
Other		—			—			900			—			900
Total fiscal 2012 charges	$	19,543		$	14,787		$	1,779		$	470		$	36,579
Recorded to cost of product sales	$	19,064		$	—		$	—		$	—		$	19,064
Recorded to restructuring	$	479		$	14,787		$	1,779		$	470		$	17,515
Fiscal 2013 charges:
Workforce reductions		—			1,792			1,489			—			3,281
Other		—			—			652			—			652
Total fiscal 2013 charges	$	—		$	1,792		$	2,141		$	—		$	3,933
Rollforward of Accrued Restructuring
Total fiscal 2012 charges	$	19,543		$	14,787		$	1,779		$	470		$	36,579
Non-cash impairment charges		(16,316	)		(585	)		—			—			(16,901	)
Stock compensation		—			(3,500	)		—			—			(3,500	)
Severance payments		(128	)		(2,423	)		—			(78	)		(2,629	)
Purchase orders and other contractual obligations payments		(2,572	)		—			—			—			(2,572	)
Other payments		—			—			—			(430	)		(430	)
Acquired		—			83			—			—			83
Foreign exchange and other adjustments		—			22			—			91			113
Balance at September 29, 2012	$	527		$	8,384		$	1,779		$	53		$	10,743
Fiscal 2013 charges		—			1,792			2,141			—			3,933
Stock compensation		—			(222	)		—			—			(222	)
Severance payments		—			(6,775	)		—			(53	)		(6,828	)
Purchase orders and other contractual obligations payments		(527	)		—			(211	)		—			(738	)
Foreign exchange and other adjustments		—			5			—			—			5
Balance at December 29, 2012	$	—		$	3,184		$	3,709		$	—		$	6,893

Abandonment of Adiana Product Line

At the end of the second quarter of fiscal 2012, the Company decided to cease manufacturing, marketing and selling its Adiana system, which was a product line within the Company’s GYN Surgical reporting segment. Management determined that the product was not financially viable and would not become so in the foreseeable future. In addition, the Company settled its intellectual property litigation regarding the Adiana system with Conceptus, Inc., which did not result in any additional charges. In the second quarter of fiscal 2012, the Company recorded a charge of $18.3 million and recorded additional adjustments in fiscal 2012 resulting in an aggregate charge of $19.5 million. Of the total charge, $19.1 million was recorded within cost of product sales and $0.4 million was recorded in restructuring. The amount recorded in cost of product sales comprised impairment charges of $9.9 million to record inventory at its net realizable value, $6.5 million to write down certain manufacturing equipment and equipment placed at customer sites to its fair value that had no further utility, and $2.7 million for outstanding contractual purchase orders of raw materials and

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components that will not be utilized and other contractual obligations. In connection with this action, the Company terminated certain manufacturing and other personnel primarily at its Costa Rica location, resulting in severance charges of $0.1 million, and incurred other contractual charges of $0.3 million. All identified employees were terminated and paid as of September 29, 2012.

Consolidation of Diagnostics Operations

In connection with its acquisition of Gen-Probe, the Company implemented restructuring actions to consolidate its Diagnostics business, such as streamlining product development initiatives, reducing overlapping functional areas such as sales, marketing and general and administrative functions, and consolidation of manufacturing resources, field services and support. As a result, the Company terminated certain employees from Gen-Probe and its legacy diagnostics business in research and development, sales, marketing, and general and administrative functions. The Company recorded severance and benefit charges in fiscal 2012 of $13.3 million related to this action pursuant to ASC 420,Exit or Disposal Cost Obligations (ASC 420). The majority of these employees ceased working in the fourth quarter of fiscal 2012, and their full severance charge was recorded in the fourth quarter of fiscal 2012. In addition, certain of the terminated Gen-Probe employees had unvested stock options and the vesting terms were accelerated as a result of termination. As such, the severance charges in fiscal 2012 include $3.5 million of stock-based compensation expense. In the first quarter of fiscal 2013, the Company recorded $0.8 million of severance charges, including $0.2 million for stock-based compensation.

In addition, the Company is moving its legacy molecular diagnostics operations from Madison, Wisconsin to Gen-Probe’s facilities in San Diego, California. This transfer is expected to be finalized by the end of calendar 2014, and the majority of employees in Madison will be terminated in fiscal 2013 and 2014. The Company is recording severance and benefit charges pursuant to ASC 420 and estimates the total severance and benefits charge to be approximately $6.4 million, which will be recorded ratably over the estimated service period of the affected employees. The Company recorded $1.0 million in the first quarter of fiscal 2013 and $0.9 million in the fourth quarter of fiscal 2012. The Company also recorded non-cash charges of $0.6 million in the fourth quarter of fiscal 2012 as a result of exiting certain research projects. Additional charges, which are not expected to be significant, will be recorded as the manufacturing operation is transferred and the facility is closed down. These charges will be recorded as they are incurred.

Closure of Indianapolis Facility

In the fourth quarter of fiscal 2012, the Company finalized its decision to transfer production of its interventional breast products, which are included within the Breast Health reporting segment, from its Indianapolis facility to its facility in Costa Rica. The transfer is expected to be completed in the first half of calendar 2014, and all employees at the Indianapolis location will be terminated. The Company is recording severance and benefit charges pursuant to ASC 420 and estimates the total severance and benefits charge to be approximately $6.4 million, which will be recorded ratably over the estimated service period of the affected employees. The Company recorded $1.5 million of severance benefits in the first quarter of fiscal 2013 and $0.9 million in the fourth quarter of fiscal 2012. In addition, the Company recorded $0.7 million in the first quarter of fiscal 2013 for additional miscellaneous items and $0.9 million in the fourth quarter of fiscal 2012 for amounts owed to the state of Indiana for employment credits. Additional charges, which are not expected to be significant, will be recorded as the manufacturing operation is transferred and the facility is closed down. These charges will be recorded as they are incurred.

Consolidation of Selenium Panel Coating Production

During the third quarter of fiscal 2012, the Company finalized its decision to consolidate its Selenium panel coating process and transfer the production line to its Newark, Delaware facility from its Hitec-Imaging German subsidiary. This production line is included within the Breast Health segment. The transfer is expected to be completed in the second half of fiscal 2013. In connection with this consolidation plan, the Company expects to terminate certain employees, primarily manufacturing personnel. Severance charges will be recorded pursuant to ASC 420 because the severance benefits qualify as one-time employee termination benefits. Since communication of the severance benefit to the affected employees had not been made as of December 29, 2012, no charges have been recorded as of December 29, 2012. Employees must continue to be employed by the Company until their employment is involuntarily terminated in order to receive the severance benefit. As such, the severance benefit will be recognized ratably over the required service period once the individual severance benefits are known and communicated to the employees. The termination communications began in January 2013. The Company expects to incur between $1.2 million and $1.4 million for severance charges in fiscal 2013.

(5) Borrowings and Credit Arrangements

The Company had total debt with a carrying value of $5.04 billion at December 29, 2012 and September 29, 2012. The Company’s borrowings consisted of the following:

	December 29, 2012		September 29, 2012
Current debt obligations, net of debt discount:
Convertible Notes	$	734,476	$	—
Term Loan A		49,603		49,582
Term Loan B		14,858		14,853
Total current debt obligations		798,937		64,435
Long-term debt obligations, net of debt discount:
Term Loan A		930,066		942,065
Term Loan B		1,467,191		1,470,454
Senior Notes		1,000,000		1,000,000
Convertible Notes		839,828		1,558,660
Total long-term debt obligations		4,237,085		4,971,179
Total debt obligations	$	5,036,022	$	5,035,614

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Credit Agreement

Borrowings outstanding under the credit and guaranty agreement (the “Credit Agreement”) for the three months ended December 29, 2012 had a weighted average interest rate of 4.0%. The interest rates on the outstanding Term Loan A and Term Loan B borrowings at December 29, 2012 ranged from 3.21% to 4.5%. Interest expense under the Credit Agreement totaled $30.0 million for the three months ended December 29, 2012, which includes non-cash interest expense of $3.7 million related to the amortization of the deferred financing costs and accretion of the debt discount.

The Credit Agreement contains affirmative and negative covenants customarily applicable to senior secured credit facilities, including covenants restricting the ability of the Company and the guarantors, subject to negotiated exceptions, to: incur additional indebtedness and additional liens on their assets; engage in mergers or acquisitions or dispose of assets; enter into sale-leaseback transactions; pay dividends or make other distributions; voluntarily prepay other indebtedness; enter into transactions with affiliated persons; make investments; and change the nature of their businesses. The credit facilities also contain total net leverage ratio and interest coverage ratio financial covenants measured as of the last day of each fiscal quarter, which are effective in our first quarter of fiscal 2013. The Company was in compliance with the Credit Agreement’s covenants as of December 29, 2012.

The Company has evaluated the Credit Agreement for derivatives pursuant to ASC 815,Derivatives and Hedging, and identified embedded derivatives that require bifurcation as the features are not clearly and closely related to the host instrument. The embedded derivatives are a default provision, which could require additional interest payments, and provision requiring contingent payments to compensate the lenders for changes in tax deductions. The Company has determined that the fair value of these embedded derivatives was nominal as of December 29, 2012.

Senior Notes

The Company’s 6.25% senior notes due 2020 (the “Senior Notes”) mature on August 1, 2020 and bear interest at the rate of 6.25% per year, payable semi-annually on February 1 and August 1 of each year, commencing on February 1, 2013. The Company recorded interest expense of $16.0 million in the three months ended December 29, 2012, which includes non-cash interest expense of $0.4 million related to the amortization of the deferred financing costs related to the Senior Notes.

On August 1, 2012, in connection with the issuance of the Senior Notes, the Company and the Guarantors entered into an exchange and registration rights agreement with the initial purchasers of the Senior Notes. Pursuant to the terms of the registration rights agreement, the Company and the Guarantors agreed to (i) file a registration statement covering an offer to exchange the Senior Notes for a new issue of identical exchange notes registered under the Securities Act on or before 180 days from August 1, 2012, (ii) use commercially reasonable efforts to cause such registration statement to become effective, and (iii) use commercially reasonable efforts to complete the exchange prior to 270 days after August 1, 2012. The Company filed a Registration Statement on Form S-4 with the Securities and Exchange Commission on January 28, 2013. The Registration Statement has not yet been declared effective. Under certain circumstances, the Company and the Guarantors may be required to provide a shelf registration statement to cover resales of the Senior Notes.

Convertible Notes

In the first quarter of fiscal 2013, the Company has reclassified its 2007 Notes to short-term in accordance with U.S. generally accepted accounting principles as they are due on demand within one year of the balance sheet date. The holders of these notes can put them to the Company on December 13, 2013.

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The Convertible Notes and related equity components (recorded in additional paid-in-capital, net of deferred taxes) consisted of the following:

	December 29, 2012			September 29, 2012
2007 Notes principal amount	$	775,000		$	775,000
Unamortized discount		(40,524	)		(50,591	)
Net carrying amount	$	734,476		$	724,409
Equity component, net of taxes	$	233,353		$	233,353
2010 Notes principal amount	$	450,000		$	450,000
Unamortized discount		(70,199	)		(74,062	)
Net carrying amount	$	379,801		$	375,938
Equity component, net of taxes	$	60,054		$	60,054
2012 Notes principal amount	$	500,000		$	500,000
Unamortized discount		(39,973	)		(41,687	)
Net carrying amount	$	460,027		$	458,313
Equity component, net of taxes	$	49,195		$	49,195

Interest expense under the Convertible Notes is as follows:

	Three months ended
	December 29, 2012		December 24, 2011
Amortization of debt discount	$	15,644	$	18,953
Amortization of deferred financing costs		908		1,007
Non-cash interest expense		16,552		19,960
2.00% accrued interest		8,610		8,578
	$	25,162	$	28,538

(6) Commitments and Contingencies

(a) Contingent Earn-Out Payments

In connection with certain of its acquisitions, the Company has incurred the obligation to make contingent earn-out payments tied to performance criteria, principally revenue growth of the acquired businesses over a specified period. In certain circumstances, such as a change of control, a portion of these obligations may be accelerated. In addition, contractual provisions relating to these contingent earn-out obligations may include covenants to operate the businesses acquired in a manner that may not otherwise be most advantageous to the Company.

The Company made its final contingent consideration payment of $16.8 million to the former Adiana shareholders, which was net of amounts withheld for qualifying legal costs, in the first quarter of fiscal 2013.

The measurement period for the Company’s remaining contingent consideration obligation to the former shareholders of Sentinelle Medical was completed in the fourth quarter of fiscal 2012. The Company accrued $3.4 million as of September 29, 2012 and made its final payment in the first quarter of fiscal 2013.

In connection with the Company’s acquisition of Interlace in fiscal 2011, the Company has an obligation to the former stockholders to make contingent payments over a two-year period up to a maximum payout of $225.0 million based on a multiple of incremental revenue growth during the two-year period following the completion of the acquisition. Pursuant to ASC 805, the Company recorded its estimate of the fair value of the contingent consideration liability based on future revenue projections of the Interlace business under various potential scenarios and weighted probability assumptions of these outcomes. The discount rate is based on the weighted-average cost of capital of the acquired business plus a credit risk premium for non-performance risk related to the liability pursuant to ASC 820,Fair Value Measurements and Disclosures (ASC 820). This fair value measurement was based on significant inputs not observable in the market and thus represented a Level 3 measurement as defined in ASC 820. This fair value measurement is directly impacted by the Company’s estimate of future incremental revenue growth of the business. Accordingly, if actual revenue

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growth is higher or lower than the estimates within the fair value measurement, the Company would record additional charges or benefits, respectively, as appropriate. The Company recorded charges of $10.0 million and $5.6 million in the first quarter of fiscal 2013 and 2012, respectively, to record the contingent consideration liability at fair value. As of December 29, 2012, the Company has accrued $93.0 million for the contingent consideration liability to the former Interlace stockholders, which when disbursed will be net of legal indemnification holdbacks.

In connection with the Company’s acquisition of TCT, the Company has an obligation to certain of the former shareholders, based on future employment, to make contingent payments over a two year period not to exceed $200.0 million less a deferred payment of $35.0 million from the initial consideration. The first earn-out payment of $54.0 million was made in the fourth quarter of fiscal 2012. At December 29, 2012, the Company has accrued $68.5 million for the second contingent earn-out payment.

In connection with the Company’s acquisition of Healthcome, the Company has an obligation to the former shareholders to make contingent payments totaling $5.0 million over the next two fiscal years. At December 29, 2012, the Company has accrued $5.0 million for these contingent payments as employment was no longer required.

A summary of amounts recorded to the Consolidated Statements of Operations is as follows:

Statement of Operations Line Item – 3 Months Ended December 29, 2012	Interlace		TCT		Total
Contingent consideration – compensation expense	$	—	$	29,486	$	29,486
Contingent consideration – fair value adjustments		10,040		—		10,040
	$	10,040	$	29,486	$	39,526

Statement of Operations Line Item – 3 Months Ended December 24, 2011	Sentinelle Medical			Interlace		TCT		Healthcome		Total
Contingent consideration – compensation expense	$	—		$	—	$	10,012	$	429	$	10,441
Contingent consideration – fair value adjustments		(468	)		5,590		—		—		5,122
	$	(468	)	$	5,590	$	10,012	$	429	$	15,563

(b) Litigation and Related Matters

On June 9, 2010, Smith & Nephew, Inc. filed suit against Interlace, which the Company acquired on January 6, 2011, in the United States District Court for the District of Massachusetts. In the complaint, it is alleged that the Interlace MyoSure hysteroscopic tissue removal device infringes U.S. patent 7,226,459. The complaint seeks permanent injunctive relief and unspecified damages. A Markman hearing on claim construction was held on November 9, 2010, and a ruling was issued on April 21, 2011. On November 22, 2011, Smith & Nephew, Inc. filed suit against the Company in the United States District Court for the District of Massachusetts. In the complaint, it is alleged that use of the MyoSure hysteroscopic tissue removal system infringes U.S. patent 8,061,359. The complaint seeks preliminary and permanent injunctive relief and unspecified damages. On January 17, 2012, at a hearing on Smith & Nephew’s motion for preliminary injunction with respect to the suit filed on November 22, 2011, the judge did not issue an injunction, consolidated the two matters for a single trial and scheduled a trial on the merits for both claims for June 25, 2012. A case management conference held on February 14, 2012 resulted in the trial being rescheduled to begin on August 20, 2012. On March 15, 2012, the Court heard summary judgment arguments related to the ‘459 patent and claim construction arguments related to the ‘359 patent. On June 5, 2012, the Court denied Smith & Nephew’s request for summary judgment of infringement, denied Smith & Nephew’s request for preliminary injunction, and denied the Company’s requests for summary judgment of non-infringement and invalidity. On September 4, 2012, following a two week trial, the jury returned a verdict of infringement of both the ‘459 and ‘359 patents and assessed damages of $4.0 million. The court has not yet entered judgment adopting the jury’s finding. Based in part on the fact the United States Patent and Trademark Office (“USPTO) has taken up a re-examination of both the ‘359 and ‘459 patents rejecting all previously issued claims, including all claims asserted against the MyoSure product, the Company has filed post trial motions seeking to reverse the jury’s rulings. A bench trial regarding the Company’s assertion of inequitable conduct on the part of Smith & Nephew with regard to the ‘359 was held on December 9, 2012. A hearing on post-trial motions for that trial is scheduled for February 7, 2013. At this time, based on available information regarding this litigation, the Company does not believe a loss is probable and is unable to reasonably assess the ultimate outcome of this case or determine an estimate, or a range of estimates, of potential losses, beyond the pending jury verdict. The purchase and sale agreement associated with the acquisition of Interlace includes an indemnification provision that provides for the reimbursement of a portion of legal expenses in defense of the Interlace intellectual property. The Company has the right to collect certain amounts set aside in escrow and, as applicable, offset contingent consideration payments of qualifying legal costs. The Company is recording legal fees incurred for this suit pursuant to the indemnification provision net within accrued expenses.

        On February 10, 2012, C.R. Bard (as acquirer of SenoRx, Inc. “SenoRx”) filed suit against the Company in the United States District Court for the District of Delaware. In the complaint, it is alleged that the Company’s MammoSite product infringes SenoRx’s U.S. Patents 8,079,946 and 8,075,469. The complaint seeks permanent injunctive relief and unspecified damages. On September 4, 2012 and October 16, 2012 the USPTO took up a re-examination of the ‘946 and ‘469 patents respectively. With respect to the ‘469 patent, all previously issued claims were rejected and for the ‘846 patent all but four claims were rejected. Based on the actions of the USPTO, the Company has filed a motion seeking to stay all litigation proceedings pending the outcome of the USPTO’s re-examination of both patents in suit. On January 11, 2013 the court issued an order denying the stay. At this time, based on available information regarding this litigation, the Company is unable to reasonably assess the ultimate outcome of this case or determine an estimate, or a range of estimates, of potential losses.

On March 6, 2012, Enzo Life Sciences, Inc. (“Enzo”) filed suit against the Company in the United States District Court for the District of Delaware. In the complaint, it is alleged that certain of the Company’s molecular diagnostics products, including without limitation products based on its proprietary Invader chemistry such as Cervista HPV high risk and Cervista HPV 16/18, infringe Enzo’s U.S. Patent 6,992,180. The complaint seeks permanent injunctive relief and unspecified damages. The Company was formally served with the complaint on July 3, 2012, but no hearing has been scheduled. In January 2012, Enzo filed suit against Gen-Probe in the United States District Court for the District of Delaware. In that complaint, it is alleged that certain of Gen-Probe’s diagnostics products, including products that incorporate Gen-Probe’s patented HPA technology, such as the APTIMA Combo 2 and APTIMA HPV assays, infringe Enzo’s U.S. Patent 6,992,180. The complaint seeks permanent injunctive relief and unspecified damages. At this time, based on available information regarding this litigation, the Company is unable to reasonably assess the ultimate outcome of this case or determine an estimate, or a range of estimates, of potential losses.

Prior to its acquisition by Hologic, Gen-Probe had patent infringement claims against Becton Dickinson (“BD”) seeking monetary damages and injunctive relief. The parties settled this litigation in the first quarter of fiscal 2013. Under the terms of the settlement, BD made a one-time payment and was granted a non-exclusive royalty-bearing license to the asserted intellectual property.

A number of lawsuits have been filed against the Company, Gen-Probe, and Gen-Probe’s board of directors. These include: (1) Teamsters Local Union No. 727 Pension Fund v. Gen-Probe Incorporated, et al. (Superior Court of the State of California for the County of San Diego); (2) Timothy Coyne v. Gen-Probe Incorporated, et al. (Delaware Court of Chancery); and (3) Douglas R. Klein v. John W. Brown, et al. (Delaware Chancery Court). The two Delaware actions have been consolidated into a single action titled: In re: Gen-Probe Shareholders Litigation. The suits were filed after the announcement of our acquisition of Gen-Probe on April 30, 2012 as putative stockholder class actions. Each of the actions assert similar claims alleging that Gen-Probe’s board of directors failed to adequately discharge its fiduciary duties to shareholders by failing to adequately value Gen-Probe’s shares and ensure that Gen-Probe’s shareholders received adequate consideration in our acquisition of Gen-Probe, that the acquisition was the product of a flawed sales process, and that the Company aided and abetted the alleged breach of fiduciary duty. The plaintiffs demand, among other things, a preliminary and permanent injunction enjoining our acquisition of Gen-Probe and rescinding the transaction or any part thereof that has been implemented. On May 24, 2012, the plaintiffs in the Delaware action filed an amended complaint, adding allegations that the disclosures in Gen-Probe’s preliminary proxy statement were inadequate. The defendants in the Delaware action answered the complaint on June 4, 2012. On July 18, 2012, the parties in the Delaware action entered into a memorandum of understanding regarding a proposed settlement of the litigation. The proposed settlement is conditioned upon, among other things, the execution of an appropriate stipulation of settlement, consummation of the merger, and final approval of the proposed settlement by the Delaware Court of Chancery. On July 9, 2012, the plaintiffs in the California action filed a motion for voluntary dismissal without prejudice. On July 12, 2012, the California Superior Court entered an order dismissing the California complaint without prejudice.

The Company is a party to various other legal proceedings and claims arising out of the ordinary course of its business. The Company believes that except for those described above there are no other proceedings or claims pending against it the ultimate resolution of which would have a material adverse effect on its financial condition or results of operations. In all cases, at each reporting period, the Company evaluates whether or not a potential loss amount or a potential range of loss is probable and reasonably estimable under ASC 450,Contingencies. Legal costs are expensed as incurred.

(7) Sale of Makena

On January 16, 2008, the Company entered into an agreement to sell the full world-wide rights of its Makena (formerly Gestiva) pharmaceutical product to K-V Pharmaceutical Company (“KV”) upon FDA approval of the then pending Makena new drug application for $82.0 million. The Company executed certain amendments to this agreement resulting in an increase of the total sales price to $199.5 million and changing the timing of when payments are due to the Company. Gains attributable to payments in the amount of $79.5 million received from KV prior to FDA approval were deferred.

        On February 3, 2011, the Company received FDA approval of Makena, and subject to a security interest and a right of reversion for failure to make future payments, all rights to Makena were transferred to KV. Upon FDA approval, the Company received $12.5 million, and including the $79.5 million previously received, the Company recorded a gain on the sale of intellectual property, net of the write-off of certain assets, of $84.5 million in the second quarter of fiscal 2011. Pursuant to the amended agreement, the Company received $12.5 million in the second quarter of fiscal 2012, which was recorded net of amounts due to the inventor of Makena. The Company was to receive the remaining $95.0 million of the sales price over a period of 18 to 30 months from FDA approval (subject to further deferral elections) depending on which one of two payment options KV selected. KV would also have owed the Company a 5% royalty on sales for certain time periods determined based upon the payment option or deferral elections selected by KV. On August 4, 2012, KV and certain of its subsidiaries filed voluntary petitions for reorganization under Chapter 11 of Title 11 of the United States Code in the United States Bankruptcy Court for the Southern District of New York. The Company had been pursuing its claims against KV in these proceedings for amounts due to the Company under its agreement with KV, and in December 2012, the

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Company and KV executed a settlement agreement, which became effective on December 28, 2012 upon the Bankruptcy Court entering certain orders. Under the settlement agreement, the Company released KV from all claims in consideration of a $60.0 million payment. The Company recorded this amount in the first quarter of fiscal 2013, net of certain costs, including contingent fees and amounts due to the inventor, resulting in a gain of $53.9 million. The Company will receive no further payments from KV.

(8) Marketable Securities

The Company’s marketable securities are comprised of an equity security and mutual funds. The equity security is an investment in the common stock of a publicly traded company, and the mutual funds are to fund the Gen-Probe deferred compensation plan. The equity security is classified as available-for-sale and is recorded at fair value with the unrealized gains or losses, net of tax, within accumulated other comprehensive income (loss), which is a component of stockholders’ equity. The mutual funds are classified as trading and are recorded at fair value with unrealized gains and losses recorded in other income in the Consolidated Statements of Income.

The following reconciles the cost basis to the fair market value of the Company’s one equity security as of December 29, 2012.

	Cost		Gross Unrealized Gains		Gross Unrealized Losses			Fair Value
Equity security	$	5,931	$	—	$	(459	)	$	5,472

(9) Net Income Per Share

A reconciliation of basic and diluted share amounts are as follows:

	Three Months Ended
	December 29, 2012		December 24, 2011
Basic weighted average common shares outstanding		266,344		262,717
Weighted average common stock equivalents from assumed exercise of stock options and restricted stock units		3,035		2,241
Diluted weighted average common shares outstanding		269,379		264,958
Weighted-average anti-dilutive shares related to:
Outstanding stock options		8,207		10,827
Restricted stock units		—		1,588

(10) Stock-Based Compensation

The following presents stock-based compensation expense in the Company’s Consolidated Statements of Income:

	Three Months Ended
	December 29, 2012		December 24, 2011
Cost of revenues	$	1,834	$	1,107
Research and development		1,868		1,201
Selling and marketing		2,201		1,550
General and administrative		5,941		4,799
Restructuring		222		—
	$	12,066	$	8,657

The Company granted approximately 2.1 million and 2.0 million stock options during the three months ended December 29, 2012 and December 24, 2011, respectively, with weighted average exercise prices of $19.86 and $17.02, respectively. There were 19.0 million options outstanding at December 29, 2012 with a weighted average exercise price of $17.86.

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The Company uses a binomial model to determine the fair value of its stock options. The weighted-average assumptions utilized to value these stock options are indicated in the following table:

	Three Months Ended
	December 29, 2012			December 24, 2011
Risk-free interest rate		0.5	%		0.7	%
Expected volatility		43.7	%		46.9	%
Expected life (in years)		4.4			4.3
Dividend yield		—			—
Weighted average fair value of options granted	$	7.06		$	6.41

The Company granted approximately 1.8 million and 1.5 million restricted stock units (RSU) during the three months ended December 29, 2012 and December 24, 2011, respectively, with weighted average grant date fair values of $19.86 and $17.08, respectively. As of December 29, 2012, there were 4.2 million unvested RSUs outstanding with a weighted average grant date fair value of $18.00. The Company also granted approximately 0.1 million market stock units (MSU) during the three months ended December 29, 2012 to its chief executive officer and chief financial officer. The MSUs were valued at $18.49 using the Monte Carlo simulation model. Each recipient of the MSUs is eligible to receive between zero and 200% of the target number of shares of the Company’s common stock at the end of three years provided the Company’s stock price achieves the defined measurement criteria. The Company will recognize compensation expense over the required service period, and since these are market-based awards, the compensation expense will be recognized by the Company regardless of whether the required criteria is met to receive such shares.

The Company uses the straight-line attribution method to recognize stock-based compensation expense for stock options and RSUs. The vesting term of stock options granted to employees is generally five years with annual vesting of 20% per year on the anniversary of the grant date, and RSUs granted to employees generally vest over four years with annual vesting at 25% per year on the anniversary of the grant date. The amount of stock-based compensation recognized during a period is based on the value of the portion of the awards that is ultimately expected to vest. Based on an analysis of historical forfeitures, the Company has determined a specific forfeiture rate for certain employee groups and has applied forfeiture rates ranging from 0% to 7% as of December 29, 2012. This analysis is periodically re-evaluated and forfeiture rates will be adjusted as necessary. Ultimately, the actual stock-based compensation expense recognized will only be for those stock options and RSUs that vest.

At December 29, 2012, there was $54.1 million and $66.1 million of unrecognized compensation expense related to stock options and stock units (comprised of RSUs and MSUs), respectively, to be recognized over a weighted average period of 3.5 years and 3.1 years, respectively.

(11) Other Balance Sheet Information

	December 29, 2012			September 29, 2012
Inventories
Raw materials	$	132,031		$	134,983
Work-in-process		71,994			93,218
Finished goods		141,284			138,990
	$	345,309		$	367,191
Property and equipment
Equipment and software	$	298,691		$	296,776
Equipment under customer usage agreements		260,210			249,692
Building and improvements		156,781			156,665
Leasehold improvements		73,170			71,943
Land		51,455			51,430
Furniture and fixtures		21,921			21,495
		862,228			848,001
Less – accumulated depreciation and amortization		(358,157	)		(340,003	)
	$	504,071		$	507,998

(12) Business Segments and Geographic Information

The Company has four reportable segments: Breast Health, Diagnostics, GYN Surgical and Skeletal Health. Certain reportable segments represent an aggregation of operating units within each segment. The Company measures and evaluates its reportable segments based on segment revenues and operating income (loss) adjusted to exclude the effect of non-cash charges, such as intangible asset amortization expense, contingent consideration charges, restructuring and divestiture charges and other one-time or unusual items and related tax effects.

18

Identifiable assets for the four principal operating segments consist of inventories, intangible assets including goodwill, and property and equipment. The Company fully allocates depreciation expense to its four reportable segments. The Company has presented all other identifiable assets as corporate assets. There were no intersegment revenues during the three months ended December 29, 2012 and December 24, 2011. Segment information is as follows:

	Three Months Ended
	December 29, 2012		December 24, 2011
Total revenues:
Diagnostics	$	305,916	$	154,064
Breast Health		220,808		215,352
GYN Surgical		80,909		78,545
Skeletal Health		23,729		24,750
	$	631,362	$	472,711
Operating income (loss):
Diagnostics	$	14,295	$	20,138
Breast Health		44,946		47,417
GYN Surgical		622		(5,013	)
Skeletal Health		3,366		4,217
	$	63,229	$	66,759
Depreciation and amortization:
Diagnostics	$	91,542	$	39,989
Breast Health		9,930		10,604
GYN Surgical		26,479		26,088
Skeletal Health		204		442
	$	128,155	$	77,123
Capital expenditures:
Diagnostics	$	13,853	$	7,038
Breast Health		3,580		1,569
GYN Surgical		2,745		2,749
Skeletal Health		179		457
Corporate		2,090		2,863
	$	22,447	$	14,676

	December 29, 2012		September 29, 2012
Identifiable assets:
Diagnostics	$	6,061,568	$	6,170,553
Breast Health		952,292		956,134
GYN Surgical		1,923,953		1,944,386
Skeletal Health		33,513		32,778
Corporate		1,497,229		1,373,257
	$	10,468,555	$	10,477,108

The Company had no customers with balances greater than 10% of accounts receivable as of December 29, 2012 or September 29, 2012, or any customer that represented greater than 10% of product revenues during the three months ended December 29, 2012 and December 24, 2011.

19

Products sold by the Company internationally are manufactured at both domestic and international locations. Transfers between the Company and its subsidiaries are generally recorded at amounts similar to the prices paid by unaffiliated foreign dealers. All intercompany profit is eliminated in consolidation.

The Company operates in the major geographic areas as noted in the below chart. Revenue data is based upon customer location, and internationally totaled $175.4 million and $117.5 million during the three months ended December 29, 2012 and December 24, 2011, respectively. Other than the United States, no single country accounted for more than 10% of consolidated revenues. The Company’s sales in Europe are predominantly derived from Germany, the United Kingdom and the Netherlands. The Company’s sales in Asia-Pacific are predominantly derived from China, Australia and Japan. The “All others” designation includes Canada, Latin America and the Middle East.

Revenues by geography as a percentage of total revenues are as follows:

	Three Months Ended
	December 29, 2012			December 24, 2011
United States		72	%		75	%
Europe		14	%		12	%
Asia		9	%		7	%
All others		5	%		6	%
		100	%		100	%

(13) Income Taxes

In accordance with ASC 740,Income Taxes, each interim period is considered integral to the annual period and tax expense is measured using an estimated annual effective tax rate. An entity is required to record income tax expense each quarter based on its best estimate of the annual effective tax rate for the full fiscal year and use that rate to provide for income taxes on a current year-to-date basis, as adjusted for discrete taxable events that occur during the interim period. If an entity has a year-to-date loss in an interim period and anticipates a loss for the full fiscal year; the entity should apply the estimated annual effective tax rate to record the interim tax provision applicable to the loss. If, however, the entity is unable to reliably estimate its annual effective tax rate, then the actual effective tax rate for the year-to-date may be the best annual effective tax rate estimate. For the three months ended December 29, 2012, the Company determined that it was unable to make a reliable annual effective tax rate estimate due to the rate sensitivity as it relates to its forecasted fiscal 2013 results. Therefore, the Company recorded a tax benefit for the three months ended December 29, 2012 based on the effective rate for the three months ended December 29, 2012.

The Company’s effective tax rate for the three months ended December 29, 2012 was 142.4% compared to 47.8% for the three months ended December 24, 2011. For the three months ended December 29, 2012, the tax rate benefit was primarily due to a $19.4 million valuation allowance release related to built-in capital losses, that the Company has concluded are more likely than not realizable as a result of the $53.9 million gain recorded on the Makena sale (see Note 7), partially offset by non-deductible contingent consideration compensation expense related to TCT and Interlace. For the three months ended December 24, 2011, the effective tax rate was higher than the statutory rate primarily due to non-deductible contingent compensation expense related to TCT and contingent consideration fair value adjustments for Interlace and Sentinelle Medical. The Company also established a $2.8 million valuation allowance against Canadian tax credits due to uncertainties surrounding its ability to continue to generate future taxable income to fully utilize these tax assets.

On January 2, 2013, the American Taxpayer Relief Act of 2012 was enacted which retroactively reinstated and extended the Federal Research tax credit from January 1, 2012 to December 31, 2013. As a result, the Company expects its income tax provision for the second quarter of fiscal 2013 will include a discrete tax benefit that will impact the second quarter’s income tax provision for the previously expired period from January 1, 2012 to December 31, 2012.

As of December 29, 2012, the Company has recorded $1.69 billion of net deferred tax liabilities compared to $1.76 billion at September 29, 2012. The Company’s deferred tax assets are periodically evaluated to determine their recoverability.

The Company has $56.7 million of gross unrecognized tax benefits, including interest, as of December 29, 2012. This represents the unrecognized tax that, if recognized, would reduce the Company’s effective tax rate. The Company’s policy is to recognize accrued interest and penalties related to unrecognized tax benefits and income tax liabilities within income tax expense. As of December 29, 2012, accrued interest, net of tax benefit, was $1.9 million and no penalties have been accrued.

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(14) Goodwill and Intangible Assets

Goodwill

A rollforward of goodwill activity by reportable segment from September 29, 2012 to December 29, 2012 is as follows:

	Breast Health			Diagnostics			GYN Surgical		Skeletal Health		Total
Balance at September 29, 2012	$	635,741		$	2,283,447		$	1,015,466	$	8,125	$	3,942,779
Gen-Probe acquisition adjustments		—			(1,426	)		—		—		(1,426	)
Tax adjustments		—			(67	)		—		—		(67	)
Foreign currency		(477	)		34			587		—		144
Balance at December 29, 2012	$	635,264		$	2,281,988		$	1,016,053	$	8,125	$	3,941,430

Intangible Assets

Intangible assets consisted of the following:

Description	As of December 29, 2012				As of September 29, 2012
	Gross Carrying Value		Accumulated Amortization		Gross Carrying Value		Accumulated Amortization
Developed technology	$	3,790,865	$	863,337	$	3,784,689	$	788,274
In-process research and development		220,000		—		227,000		—
Customer relationships and contracts		1,098,231		228,268		1,097,842		205,612
Trade names		238,101		66,161		240,092		60,318
Patents		11,852		7,992		11,417		7,906
Business licenses		2,597		411		2,577		344
Non-competition agreements		306		245		310		223
Totals	$	5,361,952	$	1,166,414	$	5,363,927	$	1,062,677

The estimated remaining amortization expense as of December 29, 2012 for each of the five succeeding fiscal years is as follows:

Remainder of Fiscal 2013	$	309,777
Fiscal 2014		399,147
Fiscal 2015		384,304
Fiscal 2016		370,487
Fiscal 2017		361,458

(15) Product Warranties

Product warranty activity was as follows:

	Balance at Beginning of Period		Provisions		Settlements/ Adjustments			Balance at End of Period
Three Months Ended:
December 29, 2012	$	6,179	$	3,131	$	(2,739	)	$	6,571
December 24, 2011	$	4,448	$	2,063	$	(1,624	)	$	4,887

(16) Stockholder Rights Plan

The Amended and Restated Rights Agreement between the Company and American Stock Transfer & Trust Company, as Rights Agent, dated as of April 2, 2008 (the “Rights Plan”), and all preferred share purchase rights distributed to holders of the Company’s common stock pursuant to the Rights Plan, expired by their terms on January 1, 2013. As a result, the Rights Plan is of no further force and effect.

(17) Pension and Other Employee Benefits

The Company has certain defined benefit pension plans covering the employees of its Hitec-Imaging German subsidiary (formerly AEG). As of December 29, 2012 and September 29, 2012, the Company’s pension liability was $10.0 million and $9.7

21

million, respectively, which is primarily recorded as a component of long-term liabilities in the Consolidated Balance Sheets. As of December 29, 2012 and September 29, 2012, the pension plans held no assets. The Company’s net periodic benefit cost and components thereof were not material during the three months ended December 29, 2012 and December 24, 2011.

(18) Executive Departure

On January 22, 2013, the Company announced that Carl Hull will be retiring from his role as Senior Vice President and General Manager of Diagnostics. Mr. Hull, who served as Chairman, President and Chief Executive Officer of Gen-Probe until it was acquired by Hologic in August 2012, will continue with the Company as a consultant up to mid-August 2013. As a result, the Company expects to record a charge of approximately $6.5 million in the second quarter of fiscal 2013 related to the acceleration of certain retention payments and equity awards pursuant to the original terms of the related agreements.

(19) New Accounting Pronouncements

Disclosures about Offsetting Assets and Liabilities

In December 2011, the Financial Accounting Standards Board (FASB) issued Accounting Standards Update (ASU) No. 2011-11,Disclosures about Offsetting Assets and Liabilities. ASU 2011-11 amended ASC 210,Balance Sheet,to converge the presentation of offsetting assets and liabilities between U.S. GAAP and IFRS. ASU 2011-11 requires that entities disclose both gross information and net information about both instruments and transactions eligible for offset in the statement of financial position and instruments and transactions subject to an agreement similar to a master netting arrangement. ASU 2011-11 is effective for fiscal years, and interim periods within those years, beginning after January 1, 2013, which is the Company’s fiscal year 2014. The Company is currently evaluating the impact of the adoption of ASU 2011-11 on its consolidated financial statements.

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(20) Supplemental Guarantor Condensed Consolidating Financials

The Company’s Senior Notes issued in August 2012 are fully and unconditionally and jointly and severally guaranteed by Hologic, Inc. (“Parent/Issuer”) and each of its domestic subsidiaries. The following represents the supplemental condensed financial information of Hologic, Inc. and its guarantor and non-guarantor subsidiaries, as of December 29, 2012 and September 29, 2012 and for the three months ended December 29, 2012 and December 24, 2011.

SUPPLEMENTAL CONDENSED CONSOLIDATING BALANCE SHEET

December 29, 2012

	Parent/Issuer		Guarantor Subsidiaries		Non-Guarantor Subsidiaries		Eliminations			Consolidated
ASSETS
Current assets:
Cash and cash equivalents	$	280,938	$	343,192	$	94,341	$	—		$	718,471
Restricted cash		—		—		2,094		—			2,094
Accounts receivable, net		97,922		184,137		123,647		(53	)		405,653
Inventories		75,623		199,736		70,416		(466	)		345,309
Deferred income tax assets		—		6,755		620		(7,375	)		—
Prepaid income taxes		10,352		40,317		638		—			51,307
Prepaid expenses and other current assets		21,389		11,795		12,766		—			45,950
Intercompany receivables		—		2,128,022		56,282		(2,184,304	)		—
Other current assets – assets held-for-sale		—		68,381		23,071		—			91,452
Total current assets		486,224		2,982,335		383,875		(2,192,198	)		1,660,236
Property and equipment, net		26,978		374,634		102,459		—			504,071
Intangible assets, net		22,050		4,062,809		110,679		—			4,195,538
Goodwill		279,957		3,521,565		139,908		—			3,941,430
Other assets		117,548		49,934		1,303		(1,505	)		167,280
Investment in subsidiaries		9,849,931		117,447		2,296		(9,969,674	)		—
Total assets	$	10,782,688	$	11,108,724	$	740,520	$	(12,163,377	)	$	10,468,555
LIABILITIES AND STOCKHOLDERS’ EQUITY
Current liabilities:
Accounts payable	$	26,320	$	39,548	$	10,499	$	—		$	76,367
Accrued expenses		319,073		71,485		46,157		(432	)		436,283
Deferred revenue		89,362		9,260		22,530		—			121,152
Current portion of long-term debt		798,937		—		—		—			798,937
Deferred income tax liabilities		118,986		—		—		(7,375	)		111,611
Intercompany payables		2,112,961		—		79,556		(2,192,517	)		—
Other current liabilities – assets held-for-sale		—		6,299		1,104		—			7,403
Total current liabilities		3,465,639		126,592		159,846		(2,200,324	)		1,551,753
Long-term debt, net of current portion		4,237,085		—		—		—			4,237,085
Deferred income tax liabilities		51,763		1,513,605		10,896		208			1,576,472
Deferred service obligations – long-term		7,763		2,077		9,047		(2,447	)		16,440
Other long-term liabilities		36,062		32,788		34,989		(1,410	)		102,429
Total liabilities		7,798,312		1,675,062		214,778		(2,203,973	)		7,484,179
Total stockholders’ equity		2,984,376		9,433,662		525,742		(9,959,404	)		2,984,376
Total liabilities and stockholders’ equity	$	10,782,688	$	11,108,724	$	740,520	$	(12,163,377	)	$	10,468,555

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SUPPLEMENTAL CONDENSED CONSOLIDATING BALANCE SHEET

September 29, 2012

	Parent/Issuer		Guarantor Subsidiaries			Non-Guarantor Subsidiaries		Eliminations			Consolidated
ASSETS
Current assets:
Cash and cash equivalents	$	210,028	$	269,416		$	80,986	$	—		$	560,430
Restricted cash		—		—			5,696		—			5,696
Accounts receivable, net		101,538		192,349			115,522		(76	)		409,333
Inventories		74,500		223,043			70,180		(532	)		367,191
Deferred income tax assets		13,578		—			617		(2,480	)		11,715
Prepaid income taxes		20,805		48,429	��		611		—			69,845
Prepaid expenses and other current assets		18,817		12,816			12,668		—			44,301
Intercompany receivables		—		2,094,017			55,761		(2,149,778	)		—
Other current assets – assets held-for-sale		—		67,878			26,625		—			94,503
Total current assets		439,266		2,907,948			368,666		(2,152,866	)		1,563,014
Property and equipment, net		26,928		379,702			101,368		—			507,998
Intangible assets, net		24,034		4,162,930			114,286		—			4,301,250
Goodwill		279,956		3,522,474			140,349		—			3,942,779
Other assets		112,339		49,036			2,406		(1,714	)		162,067
Investments in subsidiaries		9,782,940		101,615			2,296		(9,886,851	)		—
Total assets	$	10,665,463	$	11,123,705		$	729,371	$	(12,041,431	)	$	10,477,108
LIABILITIES AND STOCKHOLDERS’ EQUITY
Current liabilities:
Accounts payable	$	29,847	$	43,339		$	14,037	$	—		$	87,223
Accrued expenses		238,387		86,566			50,052		(2,624	)		372,381
Deferred revenue		92,234		10,307			27,147		—			129,688
Current portion of long-term debt		64,435		—			—		—			64,435
Intercompany payables		2,085,339		6,655			66,335		(2,158,329	)		—
Other current liabilities – assets held-for-sale		—		5,520			2,102		—			7,622
Total current liabilities		2,510,242		152,387			159,673		(2,160,953	)		661,349
Long-term debt, net of current portion		4,971,179		—			—		—			4,971,179
Deferred income tax liabilities		180,916		1,581,833			8,836		—			1,771,585
Deferred service obligations – long-term		7,536		1,160			7,601		(2,583	)		13,714
Other long-term liabilities		34,559		30,587			34,504		(1,400	)		98,250
Total liabilities		7,704,432		1,765,967			210,614		(2,164,936	)		7,516,077
Total stockholders’ equity		2,961,031		9,357,738			518,757		(9,876,495	)		2,961,031
Total liabilities and stockholders’ equity	$	10,665,463	$	11,123,705		$	729,371	$	(12,041,431	)	$	10,477,108

24

SUPPLEMENTAL CONDENSED CONSOLIDATING STATEMENT OF OPERATIONS

For the Three Months Ended December 29, 2012

	Parent/Issuer			Guarantor Subsidiaries			Non-Guarantor Subsidiaries			Eliminations			Consolidated
Revenues:
Product sales	$	98,043		$	379,771		$	133,075		$	(75,687	)	$	535,202
Service and other revenues		77,960			21,141			9,872			(12,813	)		96,160
		176,003			400,912			142,947			(88,500	)		631,362
Costs and expenses:
Cost of product sales		53,520			163,895			81,765			(75,687	)		223,493
Cost of product sales – amortization of intangible assets		1,306			72,917			1,064			—			75,287
Cost of service and other revenues		38,378			15,591			9,753			(12,813	)		50,909
Research and development		7,418			41,753			2,338			—			51,509
Selling and marketing		20,773			47,365			26,305			—			94,443
General and administrative		15,320			31,016			8,055			—			54,391
Amortization of intangible assets		678			26,649			1,199			—			28,526
Contingent consideration – compensation expense		29,486			—			—			—			29,486
Contingent consideration – fair value adjustments		10,040			—			—			—			10,040
Gain on sale of intellectual property, net		—			(53,884	)		—			—			(53,884	)
Restructuring charges		221			3,286			426			—			3,933
		177,140			348,588			130,905			(88,500	)		568,133
Income from operations		(1,137	)		52,324			12,042			—			63,229
Investment and interest income		131			42			87			—			260
Interest expense		(71,254	)		(314	)		(513	)		—			(72,081	)
Other income (expense), net		119			(4,046	)		5,180			(14	)		1,239
(Loss) income before income taxes		(72,141	)		48,006			16,796			(14	)		(7,353	)
(Benefit) provision for income taxes		(11,747	)		(3,114	)		4,390			—			(10,471	)
Equity in earnings (losses) of subsidiaries		63,512			10,934			—			(74,446	)		—
Net income (loss)	$	3,118		$	62,054		$	12,406		$	(74,460	)	$	3,118

25

SUPPLEMENTAL CONDENSED CONSOLIDATING STATEMENT OF OPERATIONS

For the three Months Ended December 24, 2011

	Parent/Issuer			Guarantor Subsidiaries			Non-Guarantor Subsidiaries			Eliminations			Consolidated
Revenues:
Product sales	$	105,761		$	250,448		$	102,534		$	(66,647	)	$	392,096
Service and other revenues		73,428			14,526			7,262			(14,601	)		80,615
		179,189			264,974			109,796			(81,248	)		472,711
Costs and expenses:
Cost of product sales		53,690			80,721			64,180			(66,647	)		131,944
Cost of product sales – amortization of intangible assets		1,305			42,910			1,956			—			46,171
Cost of service and other revenues		39,235			13,730			6,862			(14,601	)		45,226
Research and development		7,244			18,130			2,968			—			28,342
Selling and marketing		16,497			42,246			18,717			—			77,460
General and administrative		13,020			24,190			9,285			—			46,495
Amortization of intangible assets		677			13,859			306			—			14,842
Contingent consideration – compensation expense		10,441			—			—			—			10,441
Contingent consideration – fair value adjustments		5,122			—			—			—			5,122
Restructuring charges		—			—			(91	)		—			(91	)
		147,231			235,786			104,183			(81,248	)		405,952
Income from operations		31,958			29,188			5,613			—			66,759
Investment and interest income		578			46			38			—			662
Interest expense		(28,709	)		(327	)		(473	)		—			(29,509	)
Other income, net		1,464			21			507			—			1,992
Income before income taxes		5,291			28,928			5,685			—			39,904
Provision for income taxes		6,209			8,571			4,312			—			19,092
Equity in earnings (losses) of subsidiaries		21,730			3,390			557			(25,677	)		—
Net income (loss)	$	20,812		$	23,747		$	1,930		$	(25,677	)	$	20,812

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SUPPLEMENTAL CONDENSED CONSOLIDATING STATEMENTS OF COMPREHENSIVE (LOSS) INCOME

For the Three Months Ended December 29, 2012

	Parent/Issuer		Guarantor Subsidiaries			Non-Guarantor Subsidiaries		Eliminations			Consolidated
Net income (loss)	$	3,118	$	62,054		$	12,406	$	(74,460	)	$	3,118
Change in cumulative translation adjustment		—		577			1,392		—			1,969
Unrealized loss on available-for-sale security		—		(557	)		—		—			(557	)
Comprehensive income (loss)	$	3,118	$	62,074		$	13,798	$	(74,460	)	$	4,530

For the Three Months Ended December 24, 2011

	Parent/Issuer		Guarantor Subsidiaries			Non-Guarantor Subsidiaries			Eliminations			Consolidated
Net income (loss)	$	20,812	$	23,747		$	1,930		$	(25,677	)	$	20,812
Change in cumulative translation adjustment		36		(188	)		(206	)		—			(358	)
Comprehensive income (loss)	$	20,848	$	23,559		$	1,724		$	(25,677	)	$	20,454

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CONSOLIDATING STATEMENT OF CASH FLOWS

For the Three Months Ended December 29, 2012

	Parent/Issuer			Guarantor Subsidiaries			Non-Guarantor Subsidiaries			Eliminations		Consolidated
OPERATING ACTIVITIES
Net cash provided by operating activities	$	112,839		$	30,075		$	12,111		$	—	$	155,025
INVESTING ACTIVITIES
Payment of additional acquisition consideration		(16,808	)		—			—			—		(16,808	)
Proceeds from sale of business, net		—						1,488			—		1,488
Proceeds from sale of intellectual property		—			60,000			—			—		60,000
Purchase of property and equipment		(2,887	)		(6,037	)		(2,309	)		—		(11,233	)
Increase in equipment under customer usage agreements		(286	)		(7,172	)		(3,756	)		—		(11,214	)
Purchase of insurance contracts		(4,000	)		—			—			—		(4,000	)
Purchase of cost-method investments		(3,400	)		(225	)		—			—		(3,625	)
(Increase) decrease in other assets		(1,967	)		(478	)		3,589			—		1,144
Net cash provided by (used in) investing activities		(29,348	)		46,088			(988	)		—		15,752
FINANCING ACTIVITIES
Repayment of long-term debt		(16,250	)		—			—			—		(16,250	)
Payment of contingent consideration		(3,408	)		—			—			—		(3,408	)
Net proceeds from issuance of common stock pursuant to employee stock plans		12,777			—			—			—		12,777
Excess tax benefit related to equity awards		2,185			—			—			—		2,185
Payment of employee restricted stock minimum tax withholdings		(7,885	)		—			—			—		(7,885	)
Net cash used in financing activities		(12,581	)		—			—			—		(12,581	)
Effect of exchange rate changes on cash and cash equivalents		—			(2,387	)		2,232			—		(155	)
Net increase in cash and cash equivalents		70,910			73,776			13,355			—		158,041
Cash and cash equivalents, beginning of period		210,028			269,416			80,986			—		560,430
Cash and cash equivalents, end of period	$	280,938		$	343,192		$	94,341		$	—	$	718,471

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CONSOLIDATING STATEMENT OF CASH FLOWS

For the Three Months Ended December 24, 2011

	Parent/Issuer			Guarantor Subsidiaries			Non-Guarantor Subsidiaries			Eliminations		Consolidated
OPERATING ACTIVITIES
Net cash provided by (used in) operating activities	$	108,796		$	7,101		$	(4,166	)	$	—	$	111,731
INVESTING ACTIVITIES
Payment of additional acquisition consideration		(9,784	)		—			—			—		(9,784	)
Purchase of property and equipment		(3,799	)		(1,500	)		(1,491	)		—		(6,790	)
Increase in equipment under customer usage agreements		—			(5,558	)		(2,328	)		—		(7,886	)
Purchase of cost-method investment		—			(150	)		—			—		(150	)
Decrease in restricted cash		—			—			9			—		9
Net cash used in investing activities		(13,583	)		(7,208	)		(3,810	)		—		(24,601	)
FINANCING ACTIVITIES
Payment of contingent consideration		(4,105	)		—			—			—		(4,105	)
Net proceeds from issuance of common stock pursuant to employee stock plans		1,627			—			—			—		1,627
Excess tax benefit related to equity awards		1,725			—			—			—		1,725
Payment of employee restricted stock minimum tax withholdings		(5,561	)		—			—			—		(5,561	)
Net cash used in financing activities		(6,314	)		—			—			—		(6,314	)
Effect of exchange rate changes on cash and cash equivalents		—			107			(173	)		—		(66	)
Net increase (decrease) in cash and cash equivalents		88,899			—			(8,149	)		—		80,750
Cash and cash equivalents, beginning of period		644,697			—			67,635			—		712,332
Cash and cash equivalents, end of period	$	733,596		$	—		$	59,486		$	—	$	793,082

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Item 2. Management’s Discussion and Analysis of Financial Condition and Results of Operations

CAUTIONARY STATEMENT

Some of the statements contained in this report are forward-looking statements within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934. These statements involve known and unknown risks, uncertainties and other factors which may cause our or our industry’s actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. Forward-looking statements include, but are not limited to, statements regarding:

• the effect of the continuing worldwide macroeconomic uncertainty on our business and results of operation;

• the coverage and reimbursement decisions of third-party payors relating to the use of our products and treatments;

• the uncertainty of the impact of cost containment efforts and federal healthcare reform legislation on our business and results of operation;

• the anticipated impact of the U.S. excise tax on the sale of most medical devices, which is effective on January 1, 2013, on our business and results of operations;

• the impact and anticipated benefits of the acquisition of Gen-Probe and the challenges associated with successfully integrating and operating the Gen-Probe business;

• the impact and anticipated benefits of other recently completed acquisitions and acquisitions we may complete in the future;

• the ability to consolidate certain of our manufacturing and other operations on a timely basis and within budget, without disrupting our business and to achieve anticipated cost synergies in connection therewith;

• our goal of expanding our market positions;

• the development of new competitive technologies and products;

• regulatory approval and clearances for our products;

• production schedules for our products;

• the anticipated development of our markets and the success of our products in these markets;

• the anticipated performance and benefits of our products;

• business strategies;

• estimated asset and liability values;

• the impact and costs and expenses of any litigation we may be subject to now or in the future;

• our compliance with covenants contained in our indebtedness;

• anticipated trends relating to our financial condition or results of operations; and

• our capital resources and the adequacy thereof.

In some cases, you can identify forward-looking statements by terms such as “may,” “will,” “should,” “could,” “would,” “expects,” “plans,” “anticipates,” “believes,” “estimates,” “projects,” “predicts,” “potential” and similar expressions intended to identify forward-looking statements. These statements are only predictions and involve known and unknown risks, uncertainties, and other factors that may cause our actual results, levels of activity, performance, or achievements to be materially different from any future results, levels of activity, performance, or achievements expressed or implied by such forward-looking statements. Given these uncertainties, you should not place undue reliance on these forward-looking statements. Also, these forward-looking statements represent our estimates and assumptions only as of the date of this report. Except as otherwise required by law, we expressly disclaim any obligation or undertaking to release publicly any updates or revisions to any forward-looking statement contained in this offering circular to reflect any change in our expectations or any change in events, conditions or circumstances on which any of our forward-looking statements are based. Factors that could cause or contribute to differences in our future financial results include the cautionary statements set forth herein and in our filings with the Securities and Exchange Commission, including those set forth under “Risk Factors” in our Annual Report on Form 10-K for the fiscal year ended September 29, 2012. We qualify all of our forward-looking statements by these cautionary statements.

OVERVIEW

We are a leading developer, manufacturer and supplier of premium diagnostics products, medical imaging systems and surgical products with an emphasis on serving the healthcare needs of women. Our core business units are focused on breast health, diagnostics, GYN surgical, and skeletal health. On August 1, 2012, we completed our acquisition of Gen-Probe. Gen-Probe is a leader in molecular diagnostics products and services that are used primarily to diagnose human diseases and screen donated human blood. Gen-Probe is part of our Diagnostics business segment.

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Our breast health products include a broad portfolio of breast imaging and related products and accessories, including digital and film-based mammography systems, MRI breast coils, CAD for mammography and minimally invasive breast biopsy devices, breast biopsy site markers, breast biopsy guidance systems, breast imaging comfort pads, and breast brachytherapy products. Our most advanced breast imaging platform, Dimensions, utilizes a new technology called tomosynthesis to produce 3D images, as well as conventional 2D full field digital mammography images.

We offer a wide range of diagnostic products which are used primarily to aid in the diagnosis of human diseases and screen donated human blood. Our molecular diagnostics products include our APTIMA family of assays, our Proprietary Invader and TMA chemistries and advanced instrumentation (PANTHER, TIGRIS and HTA). The APTIMA family of assays is used to detect the common STDs chlamydia and gonorrhea, certain high-risk strains of HPV, and Trichomonas vaginalis, the parasite that causes trichomoniasis. Our Invader chemistry comprises molecular diagnostic reagents used for a variety of DNA and RNA analysis applications, including Cervista HPV HR, and Cervista HPV 16/18 products to assist in the diagnosis of HPV, as well as other products to diagnose cystic fibrosis, cardiovascular risk and other diseases. In fiscal 2012, we received FDA approval of assays to run on our Panther instrument including APTIMA CT/GC and Trichomonas. We are also applying for approval of APTIMA HPV and Genotyping, anticipated for later this year. Our diagnostics products also include the ThinPrep System, which is primarily used in cytology applications such as cervical cancer screening, and the Rapid Fetal Fibronectin Test, which assists physicians in assessing the risk of pre-term birth. In blood screening, we develop and manufacture the PROCLEIX family of assays, which are used to detect HIV, HCV, HBV, WNV, HAV and Parvovirus in donated human blood. These blood screening products are marketed worldwide by our blood screening collaborator, Novartis, under Novartis’ trademarks.

Our GYN surgical products include our NovaSure system and MyoSure system. The NovaSure system involves a trans-cervical procedure for the treatment of heavy menstrual bleeding. The MyoSure system is a tissue removal device that is designed to provide incision-less removal of fibroids and polyps within the uterus. At the end of the second quarter of fiscal 2012, we decided to cease manufacturing, marketing and selling our Adiana permanent contraception system determining that the product was not financially viable and would not become so in the foreseeable future.

Our skeletal health products include dual-energy X-ray bone densitometry systems, an ultrasound-based osteoporosis assessment product, and our Fluoroscan mini C-arm imaging products.

Unless the context otherwise requires, references to we, us, Hologic or our company refer to Hologic, Inc. and each of its consolidated subsidiaries.

Trademark Notice

Hologic is a trademark of Hologic, Inc. Other trademarks, logos, and slogans registered or used by Hologic and its divisions and subsidiaries in the United States and other countries include, but are not limited to, the following:

Adiana, Affirm, APTIMA, APTIMA COMBO 2, Aquilex, ATEC, Celero, Cervista, C-View, Dimensions, Eviva, Fluoroscan, Gen-Probe, Healthcome, Interlace, Invader, LIFECODES, LORAD, MammoPad, MammoSite, MultiCare, MyoSure, NovaSure, PANTHER, PROCLEIX, PreservCyt, QDR, Rapid fFN, Sahara, SecurView, Selenia, Sentinelle, Serenity, StereoLoc, Suresound, TCT, ThinPrep, THA, THS, TIGRIS, TLI IQ, and Trident.

RECENT DEVELOPMENTS

On August 1, 2012, we completed our acquisition of Gen-Probe. Such acquisition, and the significant indebtedness we incurred to fund that acquisition, subject us to risks and uncertainties described herein and under the caption “Risk Factors” in Part I, Item 1A of our Annual Report on Form 10-K for our year ended September 29, 2012.

Market acceptance of our medical products in the United States and other countries is dependent upon the purchasing and procurement practices of our customers, patient demand for our products and procedures and the reimbursement of patients’ medical expenses by government healthcare programs, private insurers or other healthcare payors. In the United States, the Centers for Medicare & Medicaid Services, known as CMS, establish coverage and reimbursement policies for healthcare providers treating Medicare and Medicaid beneficiaries. Under current CMS policies, varying reimbursement levels have been established for our products and treatments. Coverage and reimbursement policies and rates applicable to patients with private insurance are dependent upon individual private payor decisions which may not follow the policies and rates established by CMS. The use of our products and treatments outside the United States is similarly affected by coverage and reimbursement policies adopted by foreign governments and private insurance carriers. CMS has not adopted a reimbursement rate for the use of 3D tomosynthesis. We are working with governmental authorities, healthcare providers, insurance companies and other third-party payors in our efforts to secure

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reimbursement for the use of 3D tomosynthesis. However, we cannot assure that these efforts will be successful. Failure to obtain or delays in obtaining adequate reimbursement for the use of 3D tomosynthesis could adversely affect sales of our Dimensions 3D systems.

The continuing uncertainty surrounding worldwide financial markets and macroeconomic conditions has caused and may continue to cause the purchasers of medical equipment to decrease or delay their medical equipment purchasing and procurement activities. Additionally, volatility in world credit markets has caused and continues to cause our customers to experience difficulty securing the financing necessary to purchase certain of our products. Economic uncertainty and unemployment have and may continue to result in cost-conscious consumers focusing on acute care rather than wellness, which has and may continue to adversely affect demand for our products and procedures. Furthermore, governments and other third-party payors around the world facing tightening budgets could move to further reduce the reimbursement rates or the scope of coverage offered, which could adversely affect sales of our products. If the current adverse macroeconomic conditions continue, our business and prospects may be negatively impacted.

In March 2010, significant reforms to the healthcare system were adopted as law in the United States. The law includes provisions that, among other things, reduce and/or limit Medicare reimbursement, require all individuals to have health insurance (with limited exceptions) and imposes new and/or increased taxes. Specifically, the law requires the medical device industry to subsidize healthcare reform in the form of a 2.3% excise tax on United States sales of certain medical devices effective January 1, 2013. We expect that the majority of our products will fall under the government classification requiring the excise tax. Product sales in the United States represented 70% and 73% of our worldwide net product sales for the three months ended December 29, 2012 and year ended September 29, 2012, respectively.

We operate in a highly regulated industry and other governmental actions may adversely affect our business, operations or financial condition, including, without limitation: new laws, regulations or judicial decisions, or new interpretations of existing laws, regulations or decisions, related to healthcare availability, methods of delivery and payment for health care products and services; changes in the FDA and foreign regulatory approval processes that may delay or prevent the approval of new products and result in lost market opportunity; changes in FDA and foreign regulations that may require additional safety monitoring, labeling changes, restrictions on product distribution or use, or other measures after the introduction of our products to market, which could increase our costs of doing business, adversely affect the future permitted uses of approved products, or otherwise adversely affect the market for our products and treatments; new laws, regulations and judicial decisions affecting pricing or marketing practices; and changes in the tax laws relating to our operations, including those associated with the recently adopted healthcare reform law discussed above.

Professional societies, government agencies, practice management groups, private health/science foundations, and organizations involved in healthcare issues may publish guidelines, recommendations or studies to the healthcare and patient communities from time to time. Recommendations of government agencies or these other groups/organizations may relate to such matters as usage, cost-effectiveness, and use of related preventative services and treatments/therapies. Recommendations, guidelines or studies that are followed by patients and healthcare providers could result in decreased use of our products. For example, in November 2012, the American Congress of Obstetrics and Gynecologists, known as the ACOG, released updates in which they have recommended less frequent cervical cancer screening similar to guidelines released by ACOG in November 2009 and guidelines released in March 2012 by the U.S. Preventative Services Task Force, known as the USPSTF, and the American Cancer Society. However, the USPSTF recommendations now also include HPV co-testing for certain patient populations, an update from their draft guidelines in October 2011.

Over the last few years, there have been periodic significant fluctuations in foreign currencies relative to the U.S. dollar. The ongoing fluctuations of the value of the U.S. dollar, including the recent strengthening of the U.S. dollar against the Euro, may cause our products to be less competitive in international markets and may impact sales and profitability over time. Historically, a majority of our capital equipment sales to international dealers were denominated in U.S. dollars. However, more sales are now denominated in the Euro compared to the U.S. dollar for our Euro zone dealers. In addition, we have international sales, principally in our Diagnostics segment, that are denominated in foreign currencies. The value of these sales is also impacted by fluctuations in the value of the U.S. dollar. Given the uncertainty in the worldwide financial markets, foreign currency fluctuations may be significant in the future, and if the U.S. dollar continues to strengthen, we may experience a material adverse effect on our international revenues and operating results.

Acquisition of Gen-Probe Incorporated

On August 1, 2012, we completed the acquisition of Gen-Probe and acquired all of the outstanding shares of Gen-Probe. The total purchase price was $3.97 billion, which was funded through available cash and financing consisting of senior secured credit facilities and senior notes resulting in aggregate proceeds of $3.48 billion, net of discounts.

Gen-Probe, headquartered in San Diego, California, is a leader in molecular diagnostics products and services that are used primarily to diagnose human diseases and screen donated human blood. We expect this acquisition to enhance our molecular diagnostics franchise and to complement our existing portfolio of diagnostics products. Gen-Probe’s results of operations are reported within our Diagnostics reporting segment from the date of acquisition.

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The preliminary allocation of the purchase price is based on estimates of the fair value of assets acquired and liabilities assumed as of August 1, 2012. We are continuing to obtain information to finalize fair values of the acquired assets and liabilities, including tax assets and liabilities. Certain of Gen-Probe’s assets have been designated as assets held-for-sale and recorded at fair value less the estimated cost to sell such assets. These represent non-core assets to our business plan and are expected to be sold within one year of the acquisition. In the first quarter of fiscal 2013, we completed the sale of one of these asset groups for $2.2 million. On January 3, 2013, we entered into a definitive agreement to sell our LIFECODES business to Immucor for $85.0 million in cash, subject to adjustment, plus contingent payments of up to an additional $10.0 million based on future revenue results. LIFECODES sells molecular and antibody-based assays in the markers of transplant diagnostics, specialty coagulation and transfusion medicine. The transaction is subject to customary closing conditions, including expiration of the applicable waiting periods under the Hart-Scott-Rodino Antitrust Improvements Act of 1976, as amended, and an international regulatory review and is expected to close in the first half of fiscal 2013.

The Company recorded $227.0 million of in-process research and development projects related to six projects. One project, valued at $7.0 million, received FDA approval in October 2012, and another project, valued at $27.0 million received FDA approval in January 2013. The other projects are expected to be completed within the next 6 months to 42 months with a total estimated cost of approximately $51 million to complete such projects. Given the uncertainties inherent with product development and introduction, we cannot assure that any of our product development efforts will be successful, completed on a timely basis or within budget, if at all.

RESULTS OF OPERATIONS

All dollar amounts in tables are presented in thousands.

Product Sales

	Three Months Ended
	December 29, 2012					December 24, 2011					Change
	Amount		% of Total Revenue			Amount		% of Total Revenue			Amount			%
Product Sales
Diagnostics	$	296,538		47	%	$	152,195		32	%	$	144,343			95	%
Breast Health		141,277		22	%		144,454		31	%		(3,177	)		(2	)%
GYN Surgical		80,556		13	%		78,149		16	%		2,407			3	%
Skeletal Health		16,831		3	%		17,298		4	%		(467	)		(3	)%
	$	535,202		85	%	$	392,096		83	%	$	143,106			36	%

Diagnostics product sales increased 95% in the current quarter compared to the corresponding period in the prior year primarily due to the inclusion of Gen-Probe’s product sales (acquired in the fourth quarter of fiscal 2012), which contributed $140.4 million in revenue, and an increase of $4.4 million from our legacy molecular diagnostics products, which includes our HPV products, as we continue to gain new customer accounts and unit sales to existing customers and increase our international sales through TCT. The inclusion of Gen-Probe’s results is partially impacted by the Novartis collaboration. Pursuant to the collaboration, a portion of Gen-Probe’s revenue is contingent on donations testing revenue earned by Novartis, however, Gen-Probe recognizes the full product cost upon shipment. As a result, amounts to be received for this contingent revenue related to inventory on hand and not yet utilized by Novartis’ customers as of the acquisition date were recorded as unbilled accounts receivable on the balance sheet in purchase accounting and are not recorded as revenue in our results of operations. In the current quarter, this contingent revenue of $17.1 million was not recognized in our results of operations. In addition, we experienced an increase in international sales of ThinPrep, principally from an increase in the sales price and higher volumes of ThinPrep in China, partially offset by a slight decline in domestic units sold.

Breast Health product sales decreased 2% in the current quarter compared to the corresponding period in the prior year. In the current three month period, our digital mammography systems revenue decreased $1.5 million compared to the corresponding period in the prior year due to a decrease in the number of Selenia systems sold, primarily in the United States, a slight deterioration of average selling prices, and a continued shift in Selenia product mix and configuration differences. We have experienced the trend of selling more Selenia Performance models, which have fewer features than our base Selenia model and carry lower average selling prices than our full-featured Selenia models. In addition, we sold more Selenia systems internationally as a percentage of total Selenia systems, and average selling prices are lower in our international markets compared to the domestic market. Partially offsetting the Selenia decrease, we sold more units of our 3D Dimensions product, which have higher average selling prices than our Selenia models, in the current quarter compared to the corresponding period in the prior year. Also, we experienced a decline in sales of related components and workstations of $2.7 million in the current quarter compared to the corresponding period in the prior year. Partially offsetting the decrease in digital mammography product sales, our breast biopsy products revenue increased $1.9 million in the current quarter compared to the corresponding period in the prior year due to the increase in the number of Eviva biopsy devices sold in the United States, partially offset by a decline of ATEC devices sold worldwide.

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GYN Surgical product sales increased 3% in the current quarter compared to the corresponding period in the prior year primarily due to an increase in MyoSure system sales, including our new Aquilex fluid management system used with our MyoSure devices, of $8.1 million, partially offset by the discontinuance of Adiana system sales of $5.1 million and a decline in sales of NovaSure devices of $1.0 million. The MyoSure system was FDA approved shortly before we acquired Interlace in January 2011 and the product continues to gain strong market acceptance. The reduction in Adiana system revenues was due to our decision to cease manufacturing, marketing and selling the product as of the end of the second quarter of fiscal 2012, determining it was not financially viable and would not become so in the foreseeable future. We experienced a decrease in the number of NovaSure devices sold in the United States, which we primarily attribute to the continuing effect of unemployment and economic uncertainty, which has resulted in patients delaying surgery or opting for lower cost and generally less effective alternatives.

Skeletal Health product sales decreased 3% in the current quarter compared to the corresponding period in the prior year primarily due to a decline of $2.0 million in our osteoporosis assessment product sales worldwide. Partially offsetting this decrease was an increase in mini C-arm sales of $1.6 million primarily due to the introduction of our new Insight FD product.

Product sales by geography as a percentage of total product sales were as follows:

	Three Months Ended
	December 29, 2012			December 24, 2011
United States		70	%		73	%
Europe		15	%		13	%
Asia		10	%		8	%
All others		5	%		6	%
		100	%		100	%

The increase in European product sales as a percent of consolidated product sales is primarily due to a higher percentage of Selenia system unit sales to total sales in Europe as well as the inclusion of Gen-Probe product sales in this region. The increase in Asian product sales as a percentage of consolidated product sales is driven by an increase in ThinPrep sales in China year over year.

Service and Other Revenues

	Three Months Ended
	December 29, 2012					December 24, 2011					Change
	Amount		% of Total Revenue			Amount		% of Total Revenue			Amount		%
Service and Other Revenues	$	96,160		15	%	$	80,615		17	%	$	15,545		19	%

Service and other revenues are primarily comprised of revenue generated from our field service organization to provide ongoing service, installation and repair of our products. Service and other revenues increased 19% in the current quarter compared to the corresponding period in the prior year primarily in our Breast Health business due to an increase in the number of service contracts driven by an increase in our installed base of our digital mammography systems, and spare parts sales. In addition, the inclusion of Gen-Probe contributed $7.7 million in the current quarter compared to the corresponding period in the prior year.

Cost of Product Sales

	Three Months Ended
	December 29, 2012					December 24, 2011					Change
	Amount		% of Product Revenue			Amount		% of Product Revenue			Amount		%
Cost of Product Sales	$	223,493		42	%	$	131,944		33	%	$	91,549		69	%
Cost of Product Sales – Amortization of Intangible Assets		75,287		14	%		46,171		12	%		29,116		63	%
	$	298,780		56	%	$	178,115		45	%	$	120,665		68	%

Product sales gross margin decreased to 44% in the current quarter compared to 55% in the corresponding period in the prior year.

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Cost of Product Sales.The cost of product sales as a percentage of product sales was 42% in the current quarter compared to 33% to the corresponding period in the prior year. Cost of product sales as a percentage of product revenues in the current quarter increased in Diagnostics and Breast Health, remained flat in Skeletal Health, and decreased in GYN Surgical compared to the corresponding period in the prior year, resulting in an overall lower gross margin rate.

The Diagnostics’ gross margin rate in the current quarter declined compared to the corresponding period in the prior year primarily due to the inclusion of Gen-Probe results, which included $29.9 million of additional costs related to the sale of acquired inventory written up to fair value in purchase accounting, higher service costs and depreciation of equipment at customer sites, unfavorable manufacturing variances and distribution costs. In addition, Gen-Probe’s gross margin since acquisition was lower than its historical gross margin rate primarily due to the purchase accounting effect on our collaboration agreement with Novartis in our blood screening business. Based on the Novartis collaboration terms, a portion of Gen-Probe’s revenue is contingent on donations testing revenue earned by Novartis, however, Gen-Probe recognizes the full product cost upon shipment. As a result, amounts to be received for this contingent revenue related to inventory on hand and not yet utilized by Novartis’ customers as of the acquisition date were recorded as unbilled accounts receivable on the balance sheet in purchase accounting and are not recorded as revenue in our results of operations. In the first quarter of fiscal 2013, this contingent revenue of $17.1 million was not recognized in our results of operations.

Breast Health experienced a decrease in gross margin in the current quarter compared to the corresponding period in the prior year primarily due to a decrease in the number of Selenia systems sold, primarily in the United States, a slight deterioration of average selling prices, and a continued shift in Selenia product mix and configuration differences. We sold more Selenia Performance models, which have fewer features than our base Selenia model and carry lower average selling prices than our full-featured Selenia models. In addition, we sold more Selenia systems internationally as a percentage of total Selenia systems, and average selling prices are lower in our international markets compared to the domestic market. We also experienced unfavorable manufacturing variances. In our breast biopsy business, the sales mix in the current quarter resulted in a lower gross margin rate as we sold more Eviva disposables and less ATEC disposables as a percentage of revenue compared to the corresponding period in the prior year. Eviva disposables carry a higher manufacturing cost and additional royalty charges. We also experienced unfavorable absorption and higher production spend for this line of business due to the transfer of production from Indianapolis to Costa Rica, resulting in production of some of our breast biopsy products at two facilities. Once the transfer is complete, production will only be in Costa Rica.

The GYN Surgical gross margin rate for the current quarter improved due to the discontinuance of the Adiana system in fiscal 2012. The Adiana system had a much lower gross margin rate compared to GYN Surgical’s other core products. In addition, the increase in MyoSure system sales and transfer of its production to Costa Rica has resulted in overall lower production costs resulting in a higher gross margin for this product.

Cost of Product Sales—Amortization of Intangible Assets. Amortization of intangible assets relates to acquired developed technology. These intangible assets are generally amortized over their estimated useful lives of between 8.5 and 20 years using a straight-line method or, if reliably determinable, based on the pattern in which the economic benefits of the assets are expected to be consumed. The economic pattern is based on undiscounted future cash flows. The increase in amortization expense in the current quarter compared to the corresponding period in the prior year is primarily due to the inclusion of Gen-Probe, which accounted for $31.7 million of additional expense.

Cost of Service and Other Revenues

	Three Months Ended
	December 29, 2012					December 24, 2011					Change
	Amount		% of Service Revenue			Amount		% of Service Revenue			Amount		%
Cost of Service and Other Revenue	$	50,909		53	%	$	45,226		56	%	$	5,683		13	%

Service and other revenues gross margin was 47% in the current quarter compared to 44% in the corresponding period in the prior year. Within our Breast Health segment, the continued conversion of a high percentage of our domestic installed base of digital mammography systems to service contracts upon expiration of the warranty period without a corresponding increase in costs to service such contracts has resulted in higher gross margins, partially offset by increased costs in our Diagnostics segment for additional expenses incurred related to our international expansion efforts.

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Operating Expenses

	Three Months Ended
	December 29, 2012						December 24, 2011						Change
	Amount			% of Total Revenue			Amount			% of Total Revenue			Amount			%
Operating Expenses
Research and development	$	51,509			8	%	$	28,342			6	%	$	23,167			82	%
Selling and marketing		94,443			15	%		77,460			16	%		16,983			22	%
General and administrative		54,391			9	%		46,495			10	%		7,896			17	%
Amortization of intangible assets		28,526			5	%		14,842			3	%		13,684			92	%
Contingent consideration – compensation expense		29,486			5	%		10,441			2	%		19,045			182	%
Contingent consideration – fair value adjustments		10,040			2	%		5,122			1	%		4,918			96	%
Gain on sale of intellectual property, net		(53,884	)		(9	)%		—			—	%		(53,884	)		(100	)%
Restructuring charges, net		3,933			1	%		(91	)		—	%		4,024			(4,422	)%
	$	218,444			35	%	$	182,611			39	%	$	35,833			20	%

Research and Development Expenses.Research and development expenses increased 82% in the current quarter compared to the corresponding period in the prior year primarily due to $24.3 million from the inclusion of Gen-Probe. Partially offsetting this increase was a decline in compensation and benefits from lower headcount in the legacy Hologic businesses. Research and development primarily reflects spending on new product development programs, regulatory compliance and clinical research and trials. At any point in time, we have a number of different research projects and clinical trials being conducted and the timing of these projects and related costs can vary period to period.

Selling and Marketing Expenses.Selling and marketing expenses increased 22% in the current quarter compared to the corresponding period in the prior year primarily due to $12.5 million from the inclusion of Gen-Probe, higher compensation and benefits from additional personnel, primarily in the GYN Surgical business segment and internationally, increased marketing spend for 3D Dimensions tomosynthesis awareness, and higher international trade show related expenses. Partially offsetting these increases were no expenditures for our direct-to-consumer advertising campaign for NovaSure, which was completed in fiscal 2012, and no expenditures related to our discontinued Adiana product.

General and Administrative Expenses.General and administrative expenses increased 17% in the current quarter compared to the corresponding period in the prior year primarily due to $15.1 million from the inclusion of Gen-Probe, integration costs related to the Gen-Probe acquisition, and higher compensation and benefits, partially offset by lower legal expenses and a settlement benefit, lower bad debt expense due to a writeoff of an international account in the first quarter of fiscal 2012, and no charges recorded for ongoing sales tax audits or acquisition transaction costs, which were recorded in the first quarter of fiscal 2012.

Amortization of Intangible Assets.Amortization of intangible assets results from customer relationships, trade names, business licenses and non-compete agreements related to our acquisitions. These intangible assets are generally amortized over their estimated useful lives of between 2 and 30 years using a straight-line method or, if reliably determinable, based on the pattern in which the economic benefits of the assets are expected to be consumed utilizing expected undiscounted future cash flows. The increase in the current quarter compared to the corresponding period in the prior year is due to the inclusion of Gen-Probe, which accounted for $13.4 million of additional expense.

Contingent Consideration—Compensation Expense. In connection with certain of our recent acquisitions, we are obligated to make contingent earn-out payments. Amounts recorded in this financial statement line item are those contingent payments that are contingent on future employment. These payments are also generally based on achieving certain performance milestones, typically incremental revenue growth, as is the case for our TCT International Co., Ltd. (“TCT”) acquisition. The amounts recorded in fiscal 2013 relate solely to TCT and, in fiscal 2012 primarily relate to TCT. The increase in expense in the current quarter compared to the corresponding period in the prior year is due to higher revenue growth from TCT, resulting in a higher payout for the second measurement period.

Contingent Consideration—Fair Value Adjustments. In connection with our acquisitions of Sentinelle Medical Inc. (“Sentinelle Medical”) and Interlace Medical, Inc. (“Interlace”), we may be required to pay future consideration that is contingent on achieving certain revenue based milestones. As of each respective acquisition date, we recorded contingent consideration liabilities for the estimated fair value of the amount we expect to pay to the former shareholders of the acquired business. This liability is not contingent on future employment and is based on future revenue projections of the respective businesses under various potential scenarios and weighted probability assumptions of these outcomes. At each reporting period, we re-measure the fair value of these liabilities and record the changes in fair value through a separate line item within our Consolidated Statements of Income. Increases or decreases in the fair value of contingent consideration liabilities can result from accretion of the liability for the passage of time, changes in discount rates, and changes in the timing, probabilities and amount of revenue estimates. The Sentinelle Medical final

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measurement period ended in the fourth quarter of fiscal 2012, and as a result the charge recorded in the first quarter of fiscal 2013 relates solely to Interlace. We recorded a charge of $10.0 million in the first quarter of fiscal 2013 reflecting an increase in the fair value of the liability due to higher estimated revenues for Interlace. In the first quarter of fiscal 2012, we recorded a net charge of $5.1 million comprised of a charge of $5.6 million for accretion of the Interlace liability partially offset by a reduction in the fair value of the Sentinelle Medical liability of $0.5 million due primarily to changes in revenue assumptions.

Gain on Sale of Intellectual Property, Net.In the first quarter of fiscal 2013, we recorded a net gain of $53.9 million related to our sale of Makena to K-V Pharmaceutical Company (“KV”). On August 4, 2012, KV and certain of its subsidiaries filed voluntary petitions for reorganization under Chapter 11 of Title 11 of the United States Code in the United States Bankruptcy Court for the Southern District of New York. At this time, KV still owed us $95.0 million. We had been pursuing our claims against KV in these proceedings for amounts due under our agreement with KV, and in December 2012, we and KV executed a settlement agreement, which became effective on December 28, 2012 upon the Bankruptcy Court entering certain orders. Under the settlement agreement, we released KV from all claims in consideration of a $60.0 million payment. We recorded this amount net of certain costs, including contingent fees and amounts due to the inventor. For additional information, please refer to Note 7 to the consolidated financial statements contained in Part I, Item 1 of this Quarterly Report.

Restructuring Charges, Net.In the fourth quarter of fiscal 2012, in connection with our acquisition of Gen-Probe, we implemented a restructuring action to consolidate our Diagnostics operations by decreasing headcount and closing our legacy molecular diagnostics operations in Madison, Wisconsin. We also finalized our decision to transfer production of our interventional breast products from our Indianapolis facility to our Costa Rica facility. Pursuant to U.S. generally accepted accounting principles, the related severance and benefit charges are being recognized ratably over the respective required employee service periods, and other charges are being recognized as incurred. In the first quarter of fiscal 2013, we recorded restructuring charges of $3.9 million comprised of $3.3 million for severance and benefits and $0.6 million of other charges. For additional information pertaining to restructuring actions and charges, please refer to Note 4 to the consolidated financial statements contained in Part I, Item 1 of this Quarterly Report.

Interest Income

	Three Months Ended
	December 29, 2012		December 24, 2011		Change
	Amount		Amount		Amount			%
Interest Income	$	260	$	662	$	(402	)		(61	)%

Interest income decreased in the current quarter compared to the corresponding period in the prior year primarily due to a decrease in average cash and cash equivalents balances.

Interest Expense

	Three Months Ended
	December 29, 2012			December 24, 2011			Change
	Amount			Amount			Amount			%
Interest Expense	$	(72,081	)	$	(29,509	)	$	(42,572	)		144	%

Interest expense consists primarily of the cash interest costs and the related amortization of the debt discount and deferred financing costs on our convertible notes, amounts borrowed under our Credit Agreement and Senior Notes. The increase in interest expense in the current quarter compared to the corresponding period in the prior year was primarily due to debt borrowed under the Credit Agreement and sale of Senior Notes in connection with our Gen-Probe acquisition in the fourth quarter of fiscal 2012. Partially offsetting this increase was lower amortization of our convertible notes’ debt discount.

Other Income, net

	Three Months Ended
	December 29, 2012		December 24, 2011		Change
	Amount		Amount		Amount			%
Other Income, net	$	1,239	$	1,992	$	(753	)		(38	)%

In the first quarter of fiscal 2013, this account was primarily comprised of net foreign currency exchange gains of $0.9 million and other miscellaneous items.

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In the first quarter of fiscal 2012, this account was primarily comprised of gains on the cash surrender value of life insurance contracts related to our Nonqualified Deferred Compensation Plan, which is driven by underlying changes in stock market valuations, of $1.4 million, and net foreign currency exchange gains of $0.6 million.

(Benefit) Provision for Income Taxes

	Three Months Ended
	December 29, 2012			December 24, 2011		Change
	Amount			Amount		Amount			%
(Benefit) Provision for Income Taxes	$	(10,471	)	$	19,092	$	(29,563	)		(155	)%

In the first quarter of fiscal 2013, we determined that we were unable to make a reliable estimate of the annual effective tax rate due to the sensitivity to the rate as it relates to our forecasted fiscal 2013 results. Therefore, we recorded a tax provision in the first quarter of fiscal 2013 based on the effective tax rate for the first quarter of fiscal 2013. The Company’s effective tax rate for the three months ended December 29, 2012 was 142.4% compared to 47.8% for the three months ended December 24, 2011. In the first quarter of fiscal 2013, the tax rate benefit was primarily due to a $19.4 million valuation allowance release related to built-in capital losses, that we have concluded are more likely than not to be realized as a result of the $53.9 million gain on the Makena sale, partially offset by non-deductible contingent consideration compensation expense related to TCT and Interlace.

For the three months ended December 24, 2011, the effective tax rate was higher than the statutory rate primarily due to non-deductible contingent compensation expense related to TCT and contingent consideration fair value adjustments for Interlace and Sentinelle Medical. The Company also established a valuation allowance against Canadian tax credits of $2.8 million due to uncertainties surrounding its ability to continue to generate future taxable income to fully utilize these tax assets.

On January 2, 2013, the American Taxpayer Relief Act of 2012 was enacted which retroactively reinstated and extended the Federal Research tax credit from January 1, 2012 to December 31, 2013. As a result, we expect our income tax provision for the second quarter of fiscal 2013 will include a discrete tax benefit that will impact the second quarter’s income tax provision for the previously expired period from January 1, 2012 to December 31, 2012.

Segment Results of Operations

We report our business as four segments: Diagnostics, Breast Health, GYN Surgical and Skeletal Health. The accounting policies of the segments are the same as those described in the Notes to the Consolidated Financial Statements included in our 2012 Annual Report on Form 10-K. We measure segment performance based on total revenues and operating income. The discussion that follows is a summary analysis of total revenues and the primary changes in operating income by segment.

Diagnostics

	Three Months Ended
	December 29, 2012			December 24, 2011			Change
	Amount			Amount			Amount			%
Total Revenues	$	305,916		$	154,064		$	151,852			99	%
Operating Income	$	14,295		$	20,138		$	(5,843	)		(29	)%
Operating Income as a % of Segment Revenue		5	%		13	%

Diagnostics revenues increased in the current quarter compared to the corresponding period in the prior year primarily due to the increase in product sales discussed above, which is primarily attributable to the inclusion of Gen-Probe.

Operating income for this business segment decreased in the current quarter compared to the corresponding period in the prior year. While gross margin in absolute dollars increased in the current quarter due primarily to the inclusion of Gen-Probe as discussed above, higher operating expenses more than offset the gross margin impact. Gross margin rate decreased to 38.0% from 57.2%, which is primarily attributable to the inclusion of Gen-Probe and additional charges related to intangible asset amortization expense of $31.7 million and the recognition of additional costs of sales as a result of inventory written up to fair value in purchase accounting of $29.9 million.

Operating expenses increased primarily due to the inclusion of Gen-Probe, which contributed $68.4 million of operating expense including amortization expense of $13.4 million, restructuring charges and integration costs, and an increase in contingent consideration expense of $19.4 million compared to the first quarter of fiscal 2012. Partially offsetting these increases was the net gain of $53.9 million related to the settlement with KV for the sale of our rights to Makena discussed above.

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Breast Health

	Three Months Ended
	December 29, 2012			December 24, 2011			Change
	Amount			Amount			Amount			%
Total Revenues	$	220,808		$	215,352		$	5,456			3	%
Operating Income	$	44,946		$	47,417		$	(2,471	)		(5	)%
Operating Income as a % of Segment Revenue		20	%		22	%

Breast Health revenues increased in the current quarter compared to the corresponding period in the prior year primarily due to the $8.6 million increase in service revenues that was substantially related to additional service contracts for the increased number of digital mammography systems in our installed base, partially offset by the reduction in product revenue discussed above.

Operating income for this business segment decreased in the current quarter compared to the corresponding period in the prior year primarily due to an increase in operating expenses in the current quarter as discussed below.

In the current quarter, while absolute gross margin dollars were flat compared to the prior year corresponding quarter, the overall gross margin rate decreased to 48.2% compared to 49.3% in the corresponding period in the prior year due primarily to the decline in product gross margin discussed above. The product gross margin rate decreased to 47.7% in the current quarter compared to 50.3% in the corresponding period in the prior year. Operating expenses increased in the current quarter compared to the corresponding period in the prior year primarily due to $2.1 million of restructuring charges related to the closure of the Indianapolis facility and the first quarter of fiscal 2012 included a benefit of $0.5 million to adjust the Sentinelle Medical contingent consideration liability to fair value.

GYN Surgical

	Three Months Ended
	December 29, 2012			December 24, 2011			Change
	Amount			Amount			Amount		%
Total Revenues	$	80,909		$	78,545		$	2,364		3	%
Operating Income (Loss)	$	622		$	(5,013	)	$	5,635		112	%
Operating Income (Loss) as a % of Segment Revenue		1	%		(6	)%

GYN Surgical revenues increased in the current quarter compared to the corresponding period in the prior year due to the increase in product sales discussed above.

Operating income for this business segment increased in the current quarter compared to the corresponding period in the prior year. Gross margin in absolute dollars increased in the current quarter due to higher sales of the MyoSure system and the discontinuance of the Adiana system discussed above. The Adiana system was costly to manufacture and had low gross margins. The gross margin rate improved to 59.7% from 55.4%. Operating expenses declined in the current quarter compared to the corresponding period in the prior year primarily due to a reduction in advertising expenditures for our NovaSure system’s direct-to-consumer advertising campaign, lower legal expenses, lower marketing and medical education expenses due to the discontinuance of the Adiana product line, and in the first quarter of fiscal 2012 we recorded charges for an ongoing sales tax audit. These decreases were partially offset by an increase in charges for the fair value adjustment to the Interlace contingent consideration liability of $4.5 million.

Skeletal Health

	Three Months Ended
	December 29, 2012			December 24, 2011			Change
	Amount			Amount			Amount			%
Total Revenues	$	23,729		$	24,750		$	(1,021	)		(4	)%
Operating Income	$	3,366		$	4,217		$	(851	)		(20	)%
Operating Income as a % of Segment Revenue		14	%		17	%

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Skeletal Health revenues decreased in the current quarter compared to the corresponding period in the prior year primarily due to the decrease in product sales discussed above and slightly lower service revenues.

Operating income decreased in the current quarter compared to the corresponding period in the prior year primarily due to the decline in sales, which reduced gross margin in absolute dollars. The gross margin rate declined to 45.0% from 46.8% in the corresponding period in the prior year due to lower sales volumes. Operating expenses remained relatively flat.

LIQUIDITY AND CAPITAL RESOURCES

At December 29, 2012, we had $108.5 million of working capital, and our cash and cash equivalents totaled $718.5 million. Our working capital decreased from $901.7 million as of September 29, 2012 due to the reclassification of our 2007 Notes and related deferred tax liabilities to short-term from long-term. Our cash and cash equivalents balance increased by $158.0 million during the first three months of fiscal 2013 due to cash generated from our operations, proceeds from settlement of our intellectual property sales agreement with KV, and net proceeds from stock option exercises partially offset by cash used in investing and financing activities primarily for capital expenditures, contingent consideration and principal payment on our term loans.

In the first three months of fiscal 2013, our operating activities provided us with $155.0 million of cash, which included net income of $3.1 million, non-cash charges for depreciation and amortization aggregating $128.2 million, the fair value adjustment related to Gen-Probe acquired inventory sold of $29.9 million, non-cash interest expense of $20.7 million related to our outstanding debt, stock-based compensation expense of $12.1 million, and a $10.0 million fair value adjustment for our Interlace contingent consideration liability. These adjustments to net income were partially offset by a decrease in net deferred tax liabilities of $70.1 million, primarily from the amortization of intangible assets, and the net gain on the sale of intellectual property of $53.9 million. Cash provided by operations included a net cash inflow of $77.5 million from changes in our operating assets and liabilities. Changes in our operating assets and liabilities were driven primarily by an increase in accrued expenses of $76.1 million, principally from an increase in income tax accruals, accrued interest on our debt, and contingent consideration, partially offset by a decrease in compensation accruals due to payments, a decrease in prepaid income taxes of $18.5 million for payments received related to Gen-Probe tax filings, and a decrease in accounts receivable of $6.9 million due to improved collections. These cash flow increases were partially offset by a decrease of accounts payable of $10.6 million, which is driven by the timing of payments, deferred revenue of $6.2 million primarily due to the recognition of arrangements which previously did not meet the criteria for revenue recognition under U.S. generally accepted accounting principles, and an increase in inventory of $6.0 million primarily due to an increase in components on hand to support higher expected sales volume.

In the first three months of fiscal 2013, our investing activities provided cash of $15.8 million. We received $60.0 million under a settlement agreement with KV related to the sale of our rights to our Makena intellectual property. Partially offsetting cash inflows was the use of cash primarily for purchases of property and equipment of $22.4 million, which consisted primarily of the placement of equipment under customer usage agreements and manufacturing equipment and computer hardware, the payment of contingent consideration to the former shareholders of Adiana of $16.8 million, the purchase of insurance contracts to fund our Nonqualified Deferred Compensation Plan of $4.0 million, and strategic cost-method equity investments of $3.6 million.

In the first three months of fiscal 2013, our financing activities used cash of $12.6 million, primarily for payments of $16.3 million under our Credit Agreement, $7.9 million for employee-related taxes withheld for the net share settlement of vested restricted stock units and $3.4 million of contingent consideration paid to the former shareholders of Sentinelle Medical. Under ASC 805,Business Combinations, the payment of contingent consideration recorded at fair value in purchase accounting as of the acquisition date is treated as a financing activity. Partially offsetting these uses of cash were proceeds of $12.8 million from the exercise of stock options.

Debt

We had total recorded debt outstanding of $5.04 billion at December 29, 2012, which is comprised of our amounts outstanding under our Credit Agreement of $2.46 billion (principal $2.48 billion), Senior Notes of $1.0 billion and Convertible Notes of $1.57 billion (principal $1.725 billion).

Credit Agreement

Concurrent with closing the Gen-Probe acquisition, on August 1, 2012, we and certain domestic subsidiaries (the “Guarantors”) entered into a credit and guaranty agreement (the “Credit Agreement”) with Goldman Sachs Bank USA, in its capacity as administrative and collateral agent, and the lenders party thereto.

The credit facilities under the Credit Agreement consist of:

• $1.0 billion senior secured tranche A term loan (“Term Loan A”) with a final maturity date of August 1, 2017;

• $1.5 billion secured tranche B term loan (“Term Loan B”) with a final maturity date of August 1, 2019; and

• $300.0 million secured revolving credit facility (“Revolving Facility”) with a final maturity date of August 1, 2017.

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The credit facilities are secured by first-priority liens on, and a first-priority security interest in, substantially all of our assets and the assets of the Guarantors, including all of the capital stock of substantially all of the U.S. subsidiaries owned by us and the Guarantors, 65% of the capital stock of certain of our first-tier foreign subsidiaries and all intercompany debt.

We are required to make scheduled principal payments under Term Loan A in increasing amounts ranging from $12.5 million per three month period beginning October 31, 2012 to $50.0 million per three month period commencing October 31, 2015, and under Term Loan B in equal installments of $3.75 million per three month period beginning on October 31, 2012 and for 27 three month periods thereafter. The remaining balance for each term loan is due at maturity. Any amounts outstanding under the Revolving Facility are due at maturity. We are required to make principal repayments first, pro rata among the term loan facilities, and second to the Revolving Facility from specified excess cash flows from operations and from the net proceeds of specified types of asset sales, debt issuances, insurance recoveries and equity offerings. Subject to certain limitations, we may voluntarily prepay any of the credit facilities without premium or penalty.

The Credit Agreement contains affirmative and negative covenants customarily applicable to senior secured credit facilities, including covenants restricting the ability of the Company and the guarantors, subject to negotiated exceptions, to: incur additional indebtedness and additional liens on their assets, engage in mergers or acquisitions or dispose of assets, enter into sale-leaseback transactions, pay dividends or make other distributions, voluntarily prepay other indebtedness, enter into transactions with affiliated persons, make investments, and change the nature of their businesses.

The credit facilities contain total net leverage ratio and interest coverage ratio financial covenants measured as of the last day of each fiscal quarter, beginning with our first quarter of fiscal 2013. The total net leverage ratio is 7.00:1.00 beginning on our fiscal quarter ending December 29, 2012, and then decreases over time to 4.00:1.00 for the quarter ending September 30, 2017 and each fiscal quarter thereafter. The interest coverage ratio is 3.25:1.00 beginning on our fiscal quarter ending December 29, 2012, and then increases over time to 3.75:1.00 for the fiscal quarter ending September 30, 2017 and each quarter thereafter. The total net leverage ratio is defined as the ratio of our consolidated net debt as of the quarter end to our consolidated adjusted EBITDA for the four-fiscal quarter period ending on the measurement date. The interest coverage ratio is defined as the ratio of our consolidated adjusted EBITDA for the prior four-fiscal quarter period ending on the measurement date to adjusted consolidated cash interest expense for the same measurement period. These terms, and the calculation thereof, are defined in further detail in the Credit Agreement. As of December 29, 2012, we were in compliance with these covenants.

Senior Notes

On August 1, 2012, we completed a private placement of $1.0 billion aggregate principal amount of our Senior Notes at an offering price of 100% of the aggregate principal amount of the Senior Notes. The Senior Notes were not registered under the Securities Act or any state securities laws, and were offered only to qualified institutional buyers in reliance on Rule 144A under the Securities Act and outside the United States in accordance with Regulation S under the Securities Act. The Senior Notes are our general senior unsecured obligations and are guaranteed on a senior unsecured basis by the Guarantors. The Senior Notes mature on August 1, 2020 and bear interest at the rate of 6.25% per year, payable semi-annually on February 1 and August 1 of each year, commencing on February 1, 2013.

We may redeem up to 35% of the aggregate principal amount of the Senior Notes with the net cash proceeds of certain equity offerings at any time and from time to time before August 1, 2015, at a redemption price equal to 106.250% of the aggregate principal amount so redeemed, plus accrued and unpaid interest, if any, to the redemption date. We also have the option to redeem the Senior Notes on or after: August 1, 2015 through July 31, 2016 at 103.125% of par; August 1, 2016 through July 31, 2017 at 102.083% of par; August 1, 2017 through July 31, 2018 at 101.042% of par; and August 1, 2018 and thereafter at 100% of par. In addition, if we undergo a change of control, as provided in the indenture, we will be required to make an offer to purchase each holder’s Senior Notes at a price equal to 101% of the aggregate principal amount of the Senior Notes, plus accrued and unpaid interest, if any, to the repurchase date.

We filed a Registration Statement on Form S-4 with the Securities and Exchange Commission on January 28, 2013 to register the Senior Notes. The Registration Statement has not yet been declared effective.

Convertible Notes

At December 29, 2012, our convertible notes, in the aggregate principal amount of $1.725 billion, are recorded at $1.57 billion, which is net of the unamortized debt discount attributed to the embedded conversion feature of the convertible notes. These notes consist of:

• $775 million of our 2.00% Convertible Senior Notes due 2037 issued in December 2007 (the “2007 Notes”);

• $450 million of our 2.00% Convertible Exchange Senior Notes due 2037 issued in November 2010 (the “2010 Notes”); and

• $500 million of our 2.00% Convertible Senior Notes due 2042 issued in March 2012 (the “2012 Notes”).

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Holders may require us to repurchase the 2007 Notes on December 13, 2013, and on each of December 15, 2017, 2022, 2027 and 2032, or upon a fundamental change, as provided in the indenture for the 2007 Notes, at a repurchase price equal to 100% of their accreted principal amount, plus accrued and unpaid interest.

Holders may require us to repurchase the 2010 Notes on each of December 15, 2016, 2020, 2025, on December 13, 2030 and on December 14, 2035 or upon a fundamental change, as provided in the indenture for the 2010 Notes, at a repurchase price equal to 100% of their accreted principal amount, plus accrued and unpaid interest.

Holders may require us to repurchase the 2012 Notes on each of March 1, 2018, 2022, 2027 and 2032, and on March 2, 2037 or upon a fundamental change, as provided in the indenture for the 2012 Notes, at a repurchase price equal to 100% of their accreted principal amount, plus accrued and unpaid interest.

We may redeem any of the 2007 Notes, 2010 Notes and 2012 Notes beginning December 13, 2013, December 19, 2016, and March 6, 2018, respectively. We may redeem all or a portion of the 2007 Notes, 2010 Notes, and 2012 Notes (i.e., in cash or a combination of cash and shares of our common stock) at a redemption price equal to 100% of their principal amount, plus accrued and unpaid interest to, but excluding, the redemption date.

We have recorded deferred tax liabilities related to the convertible notes original issuance discount, representing the spread between the cash coupon rate and the higher interest rate deductible for tax purposes. When our convertible notes are extinguished, we are required to recapture the original issuance discount previously deducted for tax purposes. The 2007 Notes first put date is December 13, 2013 and the estimated tax due if the 2007 Notes are put to us on this date is approximately $144 million.

Contingent Earn-Out Payments

In connection with certain of our acquisitions, we have incurred the obligation to make contingent earn-out payments tied to performance criteria, principally revenue growth of the acquired businesses over a specified period. In certain circumstances, such as a change of control, a portion of these obligations may be accelerated. In addition, contractual provisions relating to these contingent earn-out obligations may include covenants to operate the acquired businesses in a manner that may not otherwise be most advantageous to us. These provisions may also result in the risk of litigation relating to the calculation of the amount due or our operation of the acquired business. Such litigation could be expensive and divert management attention and resources. Our obligation to make contingent earn-out payments may also result in significant operating expenses. Depending upon the particular facts and circumstances giving rise to the payment and our previous estimates, all or a portion of these payments may be required to be expensed by us when accrued. For example, our contingent earn-out obligations payable in connection with the TCT acquisition will be fully expensed as accrued because our obligation to make these payments is conditioned on the continued employment of certain key employees of TCT.

Our contingent consideration arrangements are recorded as either additional purchase price or compensation expense if continuing employment is required to receive such payments. Pursuant to ASC 805, contingent consideration that is deemed to be part of the purchase price is recorded as a liability based on the estimated fair value of the consideration we expect to pay to the former shareholders of the acquired business as of the acquisition date. This liability is re-measured each reporting period with the change in fair value recorded through a separate line item within our Consolidated Statements of Income. Increases or decreases in the fair value of contingent consideration liabilities can result from accretion of the liability for the passage of time, changes in discount rates, and changes in the timing, probabilities and amount of revenue estimates.

In connection with our acquisition of Interlace, we have an obligation to the former stockholders to make contingent earn-out payments over a two-year period up to a maximum payout of $225.0 million based on a multiple of incremental revenue growth during the two-year period following the completion of the acquisition. This obligation is recorded at fair value pursuant to ASC 805. The first contingent payment of $51.8 million was made in fiscal 2012. At December 29, 2012, the liability for the second measurement period was recorded at $90.0 million, which is net of amounts withheld for the legal indemnification provisions under the acquisition agreement. The second contingent payment is expected to be paid in fiscal 2013.

In connection with our acquisition of TCT, we have an obligation to certain of the former shareholders, based on future employment, to make contingent earn-out payments over a two year period not to exceed $200.0 million less a deferred payment of $35.0 million, which was paid in fiscal 2012. The first contingent earn-out payment of $54.0 million was made in the fourth quarter of fiscal 2012. At December 29, 2012, we have accrued $68.5 million for the second contingent earn-out payment. We will incur additional accruals during fiscal 2013 based upon a multiple of TCT revenues over the prior year. The second contingent payment is due in the fourth quarter of fiscal 2013.

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In connection with our acquisition of Healthcome, we have an obligation to the former shareholders to make contingent payments totaling $5.0 million over the next two fiscal years. At December 29, 2012, we have accrued $5.0 million for these contingent payments.

Legal Contingencies

We are currently involved in certain legal proceedings and claims. In connection with these legal proceedings and claims, management periodically reviews estimates of potential costs to be incurred by us in connection with the adjudication or settlement, if any, of these proceedings. These estimates are developed in consultation with outside counsel and are based on an analysis of potential litigation outcomes and settlement strategies. In accordance with ASC 450,Contingencies, loss contingencies are accrued if, in the opinion of management, an adverse outcome is probable and such outcome can be reasonably estimated. It is possible that future results for any particular quarter or annual period may be materially affected by changes in our assumptions or the effectiveness of our strategies relating to these proceedings.

Future Liquidity Considerations

We believe that cash and cash equivalents, cash flow from operations and the cash available under our Revolving Facility will provide us with sufficient funds in order to fund our expected normal operations, debt payments, including interest, and contingent consideration obligations over the next twelve months. Our longer-term liquidity is contingent upon future operating performance. We may also require additional capital in the future to fund capital expenditures, repayment of debt, contingent consideration obligations, acquisitions or other investments, or to repay our convertible notes and related deferred tax liabilities. As described above, we have significant indebtedness outstanding under our Credit Agreement, Senior Notes and convertible notes. These capital requirements could be substantial. For a description of risks to our operating performance and our indebtedness, see “Risk Factors” in our Annual Report on Form 10-K for the fiscal year ended September 29, 2012.

CRITICAL ACCOUNTING POLICIES AND ESTIMATES

The discussion and analysis of our financial condition and results of operations are based upon our interim consolidated financial statements, which have been prepared in accordance with U.S. generally accepted accounting principles. The preparation of these consolidated financial statements requires us to make estimates and judgments that affect the reported amounts of assets, liabilities, revenues and expenses, and related disclosure of contingent assets and liabilities. On an on-going basis, we evaluate our estimates, including those related to revenue recognition for multiple element arrangements, allowance for doubtful accounts, reserves for excess and obsolete inventories, valuations, purchase price allocations and contingent consideration related to business combinations, expected future cash flows including growth rates, discount rates, terminal values and other assumptions used to evaluate the recoverability of long-lived assets and goodwill, estimated fair values of intangible assets and goodwill, amortization methods and periods, warranty reserves, certain accrued expenses, restructuring and other related charges, stock-based compensation, contingent liabilities, tax reserves and recoverability of our net deferred tax assets and related valuation allowance. We base our estimates on historical experience and various other assumptions that are believed to be reasonable under the circumstances. Actual results could differ from these estimates if past experience or other assumptions do not turn out to be substantially accurate. Any differences may have a material impact on our financial condition and results of operations. For a discussion of how these and other factors may affect our business, see the “Cautionary Statement” and “Recent Developments” above and “Risk Factors” in our Annual Report on Form 10-K for the fiscal year ended September 29, 2012.

The critical accounting estimates used in the preparation of our financial statements that we believe affect our more significant judgments and estimates used in the preparation of our consolidated financial statements presented in this report are described in Management’s Discussion and Analysis of Financial Condition and Results of Operations and in the Notes to the Consolidated Financial Statements included in our Annual Report on Form 10-K for the fiscal year ended September 29, 2012. There have been no material changes to our critical accounting policies or estimates from those set forth in our Annual Report on Form 10-K for the fiscal year ended September 29, 2012.

Item 3. Quantitative and Qualitative Disclosures About Market Risk.

Financial Instruments, Other Financial Instruments, and Derivative Commodity Instruments. Financial instruments consist of cash equivalents, accounts receivable, cost-method equity investments, insurance contracts and related Nonqualified Deferred Compensation Plan liability, accounts payable and debt obligations. Except for our outstanding convertible notes, the fair value of these financial instruments approximates their carrying amount. As of December 29, 2012, we have $1.725 billion of principal of convertible notes outstanding, which are comprised of our 2007 Notes with a principal of $775.0 million, our 2010 Notes with a principal of $450.0 million, and our 2012 Notes with a principal of $500.0 million. The convertible notes are recorded net of the unamortized discount on our consolidated balance sheets. The fair value of our 2007 Notes, 2010 Notes and 2012 Notes as of December 29, 2012 was approximately $771.1 million, $504.7 million and $496.3 million, respectively. Amounts outstanding under our Credit Agreement aggregating $2.48 billion aggregate principal are subject to variable rates of interest based on current market rates, and as such, we believe the carrying amount of these obligations approximates fair value. In addition, based on the recent issuance of our Senior Notes, we believe their carrying amount approximates fair value.

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Primary Market Risk Exposures. Our primary market risk exposure is in the areas of interest rate risk and foreign currency exchange rate risk. We incur interest expense on borrowing outstanding under our Convertible Notes, Senior Notes and Credit Agreement. The Convertible Notes and Senior Notes have fixed interest rates. Borrowings under our Credit Agreement bear interest at a rate per annum, at our option, initially, with respect to all loans made under Term Loan A (i) at the Base Rate plus 2.00% per annum, or (ii) at the Adjusted Eurodollar Rate (i.e., the Libor rate) plus 3.00%, and with respect to loans made under Term Loan B: (i) at the Base Rate, with a floor of 2.00%, plus 2.50%, or (ii) at the Adjusted Eurodollar Rate, with a floor of 1.00% plus 3.50%.

As of December 29, 2012, there was $2.48 billion of aggregate principal outstanding under the Credit Agreement comprised of $987.5 billion under Term Loan A and $1.5 billion under Term Loan B. Since these debt obligations are variable rate instruments, our interest expense associated with these instruments is subject to change. A 10% adverse movement (increase in Libor rate) would increase annual interest expense by less than $1.0 million due to the low current interest rate environment and the floor on our Term Loan B.

The return from cash and cash equivalents will vary as short-term interest rates change. A hypothetical 10% increase or decrease in interest rates, however, would not have a material adverse effect on our financial condition.

Foreign Currency Exchange Risk.Our international business is subject to risks, including, but not limited to: unique economic conditions, changes in political climate, differing tax structures, other regulations and restrictions, and foreign exchange rate volatility. Accordingly, our future results could be materially adversely impacted by changes in these or other factors.

We conduct business worldwide and maintain sales and service offices outside the United States as well as manufacturing facilities in Costa Rica, Germany, Canada and China. The expenses of our international offices are denominated in local currencies, except at our Costa Rica subsidiary, where the majority of the business is conducted in U.S. dollars. Our international sales are denominated in a number of currencies, primarily the Euro and U.S. dollar. Fluctuations in the foreign currency rates could affect our sales, cost of goods and operating margins and could result in exchange losses. In addition, currency devaluations can result in a loss if we hold deposits of that currency.

We believe that the operating expenses of our international subsidiaries that are incurred in local currencies will not have a material adverse effect on our business, results of operations or financial condition. Our operating results and certain assets and liabilities that are denominated in the Euro are affected by changes in the relative strength of the U.S. dollar against the Euro. Our expenses, denominated in Euros, are positively affected when the U.S. dollar strengthens against the Euro and adversely affected when the U.S. dollar weakens. However, we believe that the foreign currency exchange risk is not significant. A hypothetical 10% increase or decrease in foreign currencies that we transact in would not have a material adverse impact on our financial condition or results of operations.

Item 4. Controls and Procedures.

We maintain disclosure controls and procedures that are designed to ensure that information required to be disclosed in our Securities Exchange Act reports 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 Chief Executive Officer and Chief Financial Officer, as appropriate, to allow timely decisions regarding required disclosure. In designing and evaluating the disclosure controls and procedures, management recognized that any controls and procedures, no matter how well designed and operated, can provide only reasonable assurance of achieving the desired control objectives, as ours are designed to do, and management necessarily was required to apply its judgment in evaluating the cost-benefit relationship of possible controls and procedures.

As of December 29, 2012, we carried out an evaluation, under the supervision and with the participation of our management, including our Chief Executive Officer and Chief Financial Officer, of the effectiveness of the design and operation of our disclosure controls and procedures, as defined in Rules 13a-15(e) and 15d-15(e) under the Securities Exchange Act of 1934. Based upon that evaluation, our Chief Executive Officer and Chief Financial Officer concluded that our disclosure controls and procedures are effective.

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PART II – OTHER INFORMATION

HOLOGIC, INC.

Item 1. Legal Proceedings.

Information with respect to this Item may be found in Note 6 to the Consolidated Financial Statements in this Form 10-Q, which information is incorporated herein by reference.

Additional information on our commitments and contingencies can be found in our Annual Report on Form 10-K for our fiscal year ended September 29, 2012.

Item 1A. Risk Factors.

There are no material changes from the risk factors as previously disclosed in our Annual Report on Form 10-K for our fiscal year ended September 29, 2012.

Item 2. Unregistered Sales of Equity Securities and Use of Proceeds.

Issuer’s Purchases of Equity Securities

For the majority of restricted stock units granted, the number of shares issued on the date that the restricted stock units vest is net of the minimum statutory tax withholding requirements that we pay in cash to the appropriate taxing authorities on behalf of our employees. The following table sets forth information about deemed repurchases of our common stock to cover employee income tax withholding obligations in connection with the vesting of restricted stock units under our equity incentive plans for the three months ended December 29, 2012 (shares in thousands):

Period of Repurchase	Total Number of Shares Purchased		Average Price Paid Per Share		Total Number of Shares Purchased As Part of Publicly Announced Program
September 30, 2012 – October 27, 2012		—	$	—		—
October 28, 2012 – November 24, 2012		388		20.30		—
November 25, 2012 – December 29, 2012		—		—		—
Total		388	$	20.30		—

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Item 6. Exhibits.

(a) Exhibits

		Incorporated by Reference
Exhibit Number	Exhibit Description	Form	Filing Date/ Period End Date
10.1	Separation and Release Agreement by and between Hologic and Carl W. Hull dated as of January 22, 2013.	8-K	01/22/2013
10.2	Consulting Agreement by and between Hologic and Carl W. Hull dated as of January 22, 2013.	8-K	01/22/2013
10.3*	Form of Senior Vice President Change of Control Agreement including list of officers to whom provided.
31.1*	Certification of Hologic’s CEO pursuant to Item 601(b)(31) of Regulation S-K, as adopted pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.
31.2*	Certification of Hologic’s CFO pursuant to Item 601(b)(31) of Regulation S-K, as adopted pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.
32.1**	Certification of Hologic’s CEO pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002.
32.2**	Certification of Hologic’s CFO pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002.
101.INS	XBRL Instance Document
101.SCH	XBRL Taxonomy Extension Schema Document
101.CAL	XBRL Taxonomy Extension Calculation Linkbase Document
101.LAB	XBRL Taxonomy Extension Label Linkbase Document
101.PRE	XBRL Taxonomy Extension Presentation Linkbase Document
101.DEF	XBRL Taxonomy Extension Definition

* Filed herewith.

** Furnished herewith.

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HOLOGIC, INC.

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.

	Hologic, Inc.
	(Registrant)
Date: February 7, 2013	/S/    ROBERT A. CASCELLA
	Robert A. Cascella
	Chief Executive Officer
Date: February 7, 2013	/S/    GLENN P. MUIR
	Glenn P. Muir
	Executive Vice President, Finance and Administration, and Chief Financial Officer
	(Principal Financial Officer)

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