Document and Entity Information
Document and Entity Information - shares | 6 Months Ended | |
Jun. 30, 2015 | Jul. 17, 2015 | |
Document and Entity Information [Abstract] | ||
Entity Registrant Name | VASCULAR SOLUTIONS INC | |
Entity Central Index Key | 1,030,206 | |
Current Fiscal Year End Date | --12-31 | |
Entity Well-known Seasoned Issuer | No | |
Entity Voluntary Filers | No | |
Entity Current Reporting Status | Yes | |
Entity Filer Category | Accelerated Filer | |
Entity Common Stock, Shares Outstanding | 17,321,794 | |
Document Fiscal Year Focus | 2,015 | |
Document Fiscal Period Focus | Q2 | |
Document Type | 10-Q | |
Amendment Flag | false | |
Document Period End Date | Jun. 30, 2015 |
Consolidated Balance Sheets (un
Consolidated Balance Sheets (unaudited) - USD ($) $ in Thousands | Jun. 30, 2015 | Dec. 31, 2014 |
Current assets: | ||
Cash and cash equivalents | $ 35,839 | $ 36,461 |
Accounts receivable, net of reserves of $420 and $300 in 2015 and 2014, respectively | 19,881 | 17,105 |
Inventories | 20,002 | 15,908 |
Prepaid expenses and other | 4,784 | 5,231 |
Current portion of deferred tax assets | 4,050 | 3,681 |
Total current assets | 84,556 | 78,386 |
Property, plant and equipment, net | 31,438 | 25,665 |
Goodwill | 10,081 | 10,259 |
Intangible assets, net | 9,269 | 10,164 |
Deferred tax assets, net of current portion | 1,329 | 2,894 |
Total assets | 136,673 | 127,368 |
Current liabilities: | ||
Accounts payable | 5,946 | 4,806 |
Accrued compensation | 5,338 | 4,580 |
Accrued expenses | 3,581 | 3,016 |
Accrued royalties | 208 | 230 |
Current portion of deferred revenue | 295 | 391 |
Total current liabilities | 15,368 | 13,023 |
Long-term deferred revenue, net of current portion | 99 | 202 |
Long-term deferred tax liabilities | 817 | 803 |
Total long-term liabilities | 916 | 1,005 |
Shareholders' equity: | ||
Common stock, $0.01 per share par value: Authorized shares - 40,000,000 Issued and outstanding shares - 17,321,919 - 2015; 17,202,365 - 2014 | 173 | 172 |
Additional paid-in capital | 98,829 | 97,324 |
Accumulated other comprehensive losses | (1,116) | (725) |
Retained earnings | 22,503 | 16,569 |
Total shareholders' equity | 120,389 | 113,340 |
Total liabilities and shareholders' equity | $ 136,673 | $ 127,368 |
Consolidated Balance Sheets (u3
Consolidated Balance Sheets (unaudited) (Parenthetical) - USD ($) $ in Thousands | Jun. 30, 2015 | Dec. 31, 2014 |
Current assets: | ||
Reserves for accounts receivable | $ 420 | $ 300 |
Shareholders' equity: | ||
Common stock, par value (in dollars per share) | $ 0.01 | $ 0.01 |
Common stock, authorized shares (in shares) | 40,000,000 | 40,000,000 |
Common stock, shares issued (in shares) | 17,321,919 | 17,202,365 |
Common stock, shares outstanding (in shares) | 17,321,919 | 17,202,365 |
Consolidated Statements of Earn
Consolidated Statements of Earnings (unaudited) - USD ($) $ in Thousands | 3 Months Ended | 6 Months Ended | ||
Jun. 30, 2015 | Jun. 30, 2014 | Jun. 30, 2015 | Jun. 30, 2014 | |
Net revenue: | ||||
Product revenue | $ 37,398 | $ 30,606 | $ 71,839 | $ 60,451 |
License, royalty and collaboration revenue | 152 | 71 | 322 | 133 |
Total revenue | 37,550 | 30,677 | 72,161 | 60,584 |
Product costs and operating expenses: | ||||
Cost of goods sold | 12,660 | 10,283 | 23,956 | 19,867 |
Collaboration expenses | 46 | 20 | 100 | 31 |
Research and development | 4,202 | 3,228 | 8,270 | 6,518 |
Clinical and regulatory | 1,605 | 1,275 | 3,086 | 2,575 |
Sales and marketing | 8,461 | 7,344 | 17,193 | 15,080 |
General and administrative | 4,129 | 2,731 | 8,907 | 5,590 |
Medical device excise taxes | 395 | 353 | 770 | 698 |
Amortization of purchased technology and intangibles | 404 | 412 | 808 | 823 |
Total product costs and operating expenses | 31,902 | 25,646 | 63,090 | 51,182 |
Operating earnings | 5,648 | 5,031 | 9,071 | 9,402 |
Other earnings (expenses) | 14 | (1) | 42 | 1 |
Earnings before income taxes | 5,662 | 5,030 | 9,113 | 9,403 |
Income tax expense | (1,935) | (1,825) | (3,179) | (3,400) |
Net earnings | $ 3,727 | $ 3,205 | $ 5,934 | $ 6,003 |
Net earnings per share - basic (in dollars per share) | $ 0.22 | $ 0.19 | $ 0.35 | $ 0.36 |
Net earnings per share - diluted (in dollars per share) | $ 0.21 | $ 0.18 | $ 0.33 | $ 0.34 |
Consolidated Statements of Comp
Consolidated Statements of Comprehensive Earnings (unaudited) - USD ($) $ in Thousands | 3 Months Ended | 6 Months Ended | ||
Jun. 30, 2015 | Jun. 30, 2014 | Jun. 30, 2015 | Jun. 30, 2014 | |
Consolidated Statements of Comprehensive Earnings (unaudited) [Abstract] | ||||
Net earnings | $ 3,727 | $ 3,205 | $ 5,934 | $ 6,003 |
Other comprehensive earnings (losses), net of $0 tax: Foreign currency translation adjustments | 320 | 102 | (391) | (202) |
Comprehensive earnings | $ 4,047 | $ 3,307 | $ 5,543 | $ 5,801 |
Consolidated Statements of Com6
Consolidated Statements of Comprehensive Earnings (unaudited) (Parenthetical) - USD ($) $ in Thousands | 3 Months Ended | 6 Months Ended | ||
Jun. 30, 2015 | Jun. 30, 2014 | Jun. 30, 2015 | Jun. 30, 2014 | |
Consolidated Statements of Comprehensive Earnings (unaudited) [Abstract] | ||||
Foreign currency translation adjustments, tax | $ 0 | $ 0 | $ 0 | $ 0 |
Consolidated Statements of Cash
Consolidated Statements of Cash Flows (unaudited) - USD ($) $ in Thousands | 6 Months Ended | |
Jun. 30, 2015 | Jun. 30, 2014 | |
Operating activities | ||
Net earnings | $ 5,934 | $ 6,003 |
Adjustments to reconcile net earnings to net cash provided by operating activities: | ||
Depreciation | 2,122 | 1,564 |
Amortization | 808 | 823 |
Stock-based compensation | 2,382 | 2,144 |
Deferred taxes, net | 1,573 | 458 |
Tax benefit from stock-based awards | (360) | (775) |
Gain on disposal of equipment | 0 | (6) |
Change in accounts receivable allowance | 120 | 115 |
Changes in operating assets and liabilities: | ||
Accounts receivable | (2,908) | (1,332) |
Inventories | (4,164) | (1,596) |
Prepaid expenses and other | 495 | (715) |
Accounts payable | 1,173 | 266 |
Accrued expenses and compensation | 1,316 | 670 |
Amortization of deferred license fees and other deferred revenue | (199) | (144) |
Net cash provided by operating activities | 8,292 | 7,475 |
Investing activities | ||
Purchase of property and equipment | (5,262) | (2,302) |
Purchase of building and land | (2,748) | 0 |
Proceeds from the sale of equipment | 0 | 10 |
Net cash used in investing activities | (8,010) | (2,292) |
Financing activities | ||
Repurchase of common shares | (2,276) | (2,290) |
Tax benefit from stock-based awards | 360 | 775 |
Proceeds from the exercise of stock options and sale of stock, net of expenses | 1,041 | 1,600 |
Net cash provided by (used in) financing activities | (875) | 85 |
Increase (decrease) in cash and cash equivalents | (593) | 5,268 |
Effect of exchange rate changes on cash and cash equivalents | (29) | (7) |
Cash and cash equivalents at beginning of period | 36,461 | 30,785 |
Cash and cash equivalents at end of period | 35,839 | 36,046 |
Supplemental disclosure of cash flow | ||
Cash paid for interest | 0 | 3 |
Cash paid for taxes | $ 964 | $ 2,892 |
Basis of Presentation
Basis of Presentation | 6 Months Ended |
Jun. 30, 2015 | |
Basis of Presentation [Abstract] | |
Basis of Presentation | (1) Basis of Presentation The accompanying unaudited consolidated financial statements of Vascular Solutions, Inc. (the Company) have been prepared in accordance with generally accepted accounting principles for interim financial information and with the instructions to Form 10-Q and Regulation S-X. Accordingly, they do not include all of the information and footnotes required by generally accepted accounting principles for complete financial statements. In the opinion of management, all normal, recurring adjustments considered necessary for a fair presentation have been included. The consolidated financial statements should be read in conjunction with the audited consolidated financial statements contained in the Company’s Annual Report on Form 10-K for the year ended December 31, 2014 filed with the Securities and Exchange Commission. Interim results of operations are not necessarily indicative of the results to be expected for the full year or any other interim periods. |
Net Earnings per Share
Net Earnings per Share | 6 Months Ended |
Jun. 30, 2015 | |
Net Earnings per Share [Abstract] | |
Net Earnings per Share | (2) Net Earnings per Share In accordance with Accounting Standards Codification (ASC) 260, Earnings Per Share Weighted average common shares outstanding for the three and six months ended June 30, 2015 and 2014 were as follows: Three Months Ended June 30, Six Months Ended June 30, 2015 2014 2015 2014 (unaudited) (unaudited) Weighted average shares outstanding – basic 17,018,000 16,807,000 16,995,000 16,761,000 Weighted average shares outstanding – diluted 17,996,000 17,589,000 17,946,000 17,585,000 |
Revenue Recognition
Revenue Recognition | 6 Months Ended |
Jun. 30, 2015 | |
Revenue Recognition [Abstract] | |
Revenue Recognition | (3) Revenue Recognition In the United States, the Company sells its products and services directly to hospitals and clinics. Revenue is recognized in accordance with generally accepted accounting principles as outlined in ASC 605-10-S99, Revenue Recognition In all international markets, the Company sells its products to international distributors which subsequently resell the products to hospitals and clinics. The Company has agreements with each of its distributors which provide that title and risk of loss pass to the distributor upon shipment of the products to the distributor. The Company warrants that its products are free from manufacturing defects at the time of shipment to the distributor. Revenue is recognized upon shipment of products to distributors following the receipt and acceptance of a distributor’s purchase order and is reported on a gross basis. Allowances are provided for estimated returns and costs at the time of shipment. Sales and use taxes are reported on a net basis, excluding them from revenue. The Company’s revenues from license agreements and research collaborations are recognized when earned. In accordance with ASC 605, for revenues which contain multiple deliverables, the Company separates the deliverables into separate accounting units if they meet the following criteria: (i) the delivered items have a stand-alone value to the customer; (ii) the fair value of any undelivered items can be reliably determined; and (iii) if the arrangement includes a general right of return, delivery of the undelivered items is probable and substantially controlled by the seller. Deliverables that do not meet these criteria are combined with one or more other deliverables into one accounting unit. Revenue from each accounting unit is recognized based on the applicable accounting literature, primarily ASC 605. The Company currently has a license agreement with King Pharmaceuticals, Inc. (King), now a subsidiary of Pfizer, Inc., under which the Company licensed the exclusive rights of Thrombi-Pad TM ® TM Starting in January 2012, the Company began to generate revenue from selling a reprocessing service for ClosureFAST ® In addition, the Company has reviewed the provisions of ASC 808, Collaborative Arrangements In accordance with ASC 605-45-45, the Company includes shipping and handling revenues in net revenue, and shipping and handling costs in cost of goods sold. In May 2014, the Financial Accounting Standards Board (FASB) issued guidance creating ASC 606, “ Revenue from Contracts with Customers |
Inventories
Inventories | 6 Months Ended |
Jun. 30, 2015 | |
Inventories [Abstract] | |
Inventories | (4) Inventories Inventories are stated at the lower of cost (weighted average first-in, first-out method) or market. Appropriate consideration is given to deterioration, obsolescence and other factors in evaluating net realizable value. Inventories are comprised of the following: June 30, 2015 December 31, 2014 (dollars in thousands) (unaudited) Raw materials $ 8,761 $ 8,251 Work-in-process 2,039 1,139 Finished goods 9,202 6,518 $ 20,002 $ 15,908 |
Goodwill and Other Intangible A
Goodwill and Other Intangible Assets | 6 Months Ended |
Jun. 30, 2015 | |
Goodwill and Other Intangible Assets [Abstract] | |
Goodwill and Other Intangible Assets | (5) Goodwill and Other Intangible Assets The changes in the carrying amount of goodwill and acquired intangible assets for the six months ended June 30, 2015 are as follows: Goodwill Acquired Intangibles (dollars in thousands) (unaudited) Balance at December 31, 2014 $ 10,259 $ 10,164 Amortization – (808 ) Foreign currency translation adjustments (178 ) (87 ) Balance at June 30, 2015 $ 10,081 $ 9,269 |
Credit Risk and Allowance for D
Credit Risk and Allowance for Doubtful Accounts | 6 Months Ended |
Jun. 30, 2015 | |
Credit Risk and Allowance for Doubtful Accounts [Abstract] | |
Credit Risk and Allowance for Doubtful Accounts | (6) Credit Risk and Allowance for Doubtful Accounts The Company maintains allowances for doubtful accounts for estimated losses resulting from the inability of its customers to make required payments. This allowance is regularly evaluated by the Company for adequacy by taking into consideration factors such as past experience, credit quality of the customer base, age of the receivable balances, both individually and in the aggregate, and current economic conditions that may affect a customer’s ability to pay. Accounts receivable over 60 days past due are considered past due. The Company does not accrue interest on past due accounts receivable. Receivables are written off only after all collection attempts have failed and are based on individual credit evaluation and the specific circumstances of the customer. At June 30, 2015 and December 31, 2014, the allowance for doubtful accounts was $340,000 and $220,000, respectively. All product returns must be pre-approved and, if approved, customers are subject to a 20% restocking charge. The Company analyzes the rate of historical returns when evaluating the adequacy of the allowance for sales returns, which is included with the allowance for doubtful accounts on its balance sheet. At both June 30, 2015 and December 31, 2014, the sales and return allowance was $80,000. Accounts receivable are shown net of the combined total of the allowance for doubtful accounts and allowance for sales returns of $420,000 and $300,000 at June 30, 2015 and December 31, 2014, respectively. |
Concentrations of Credit and Ot
Concentrations of Credit and Other Risks | 6 Months Ended |
Jun. 30, 2015 | |
Concentrations of Credit and Other Risks [Abstract] | |
Concentrations of Credit and Other Risks | (7) Concentrations of Credit and Other Risks In the United States, the Company sells its products directly to hospitals and clinics. In all international markets, the Company sells its products to distributors who, in turn, sell to hospitals and clinics. Loss or termination of distributors, or their inability to effectively promote the Company’s products, could have a material adverse effect on the Company’s financial condition and results of operations. With respect to accounts receivable, the Company performs credit evaluations of its customers and does not require collateral. No single customer represented greater than 10% of gross accounts receivable as of either June 30, 2015 or December 31, 2014. There have been no material losses on customer receivables. Revenue by geographic destination as a percentage of total net revenue for the six month periods ended June 30, 2015 and 2014 was 77% and 83% in the United States and 23% and 17% in international markets, respectively. Revenues are attributable to countries based on location of the customer. No single customer represented greater than 10% of the total net revenue for the six months ended June 30, 2015 or 2014. |
Dependence on Key Suppliers
Dependence on Key Suppliers | 6 Months Ended |
Jun. 30, 2015 | |
Dependence on Key Suppliers [Abstract] | |
Dependence on Key Suppliers | (8) Dependence on Key Suppliers The Company purchases certain key components from single-source suppliers. Any significant component delay or interruption could require the Company to qualify new sources of supply, if available, and could have a material adverse effect on the Company’s financial condition and results of operations. King Pharmaceuticals The Company purchases its requirements for thrombin (a component in the Hemostat products) under a Thrombin-JMI Supply Agreement entered into with King on January 9, 2007. Under the terms of the Thrombin-JMI Supply Agreement, King agrees to manufacture and supply thrombin to the Company on a non-exclusive basis. The Thrombin-JMI Supply Agreement does not contain any minimum purchase requirements. King agrees to supply the Company with such quantity of thrombin as the Company may order at a fixed price throughout the term of the Thrombin-JMI Supply Agreement as adjusted for inflation, variations in potency and other factors. The Thrombin-JMI Supply Agreement has an initial term of 10 years, followed by successive automatic one-year extensions, subject to termination by the parties under certain circumstances, including: (i) termination by King without cause any time after the fifth anniversary of the date of the Thrombin-JMI Supply Agreement upon five years prior written notice to the Company, and (ii) termination by the Company without cause any time after the fifth anniversary of the date of the Thrombin-JMI Supply Agreement upon five years prior written notice to King provided that the Device Supply Agreement, which the Company also entered into with King on January 9, 2007, has expired on its terms or the parties have agreed to terminate it. |
Commitments and Contingencies
Commitments and Contingencies | 6 Months Ended |
Jun. 30, 2015 | |
Commitments and Contingencies [Abstract] | |
Commitments and Contingencies | (9) Commitments and Contingencies Governmental Proceedings On June 28, 2011, the Company received a subpoena from the U.S. Attorney’s Office for the Western District of Texas under the Health Insurance Portability & Accountability Act of 1996 (HIPAA) requesting the production of documents related to Vari-Lase products, and in particular the use of the Vari-Lase Short Kit for the treatment of perforator veins. Subsequently, the Company learned that the U.S. Attorney’s Office also had commenced a criminal investigation of the same matter. The Vari-Lase Short Kit was sold under a 510(k) clearance for the treatment of incompetence and reflux of superficial veins in the lower extremity from 2007 until it was voluntarily withdrawn from the market in July 2014 with total U.S. sales of approximately $534,000 (0.1% of the Company’s total U.S. sales for such period) and has not been the subject of any reported serious adverse clinical event. On August 14, 2012, the United States District Court for the Western District of Texas unsealed a qui tam On November 13, 2014, a criminal indictment was issued in the United States District Court for the Western District of Texas related to the Vari-Lase Short Kit investigation. The indictment alleges that the Company and its Chief Executive Officer introduced adulterated and misbranded medical devices into interstate commerce and conspired to introduce adulterated and misbranded medical devices into interstate commerce through the alleged off-label promotion of the Vari-Lase Short Kit. The Company believes the allegations are false and is contesting them vigorously. The Company intends to bring motions to dismiss the indictment on multiple grounds. If the Company’s motions are not granted, the court has set the trial to begin on February 1, 2016 in San Antonio, Texas. Defending the Company against the indictment will entail costs that are expected to be material and will require significant attention from the Company’s management. If the Company were to be convicted of the crimes alleged in the indictment, remedies could include fines, penalties, forfeitures and compliance conditions. The Company cannot estimate the amount or range of loss if the Company were to be convicted; however, it would likely be material. If the Company were to be convicted of a crime related to the delivery of an item or service under Title XVIII of the Social Security Act, or a felony related to health care fraud, it would become automatically excluded by the Department of Health and Human Services (“HHS”) from participation in U.S. government health care programs, including Medicare and Medicaid. If the Company were to be convicted of a misdemeanor related to health care fraud, it could be excluded by HHS from participation in U.S. government health care programs, including Medicare and Medicaid. Exclusion from participation in U.S. government health care programs would substantially adversely affect the Company’s ability to continue to conduct its business. Conviction of the Company’s chief executive officer of a crime under statutes related to misbranding and health care fraud could require the termination of his employment with the Company. From time to time, the Company is involved in additional legal proceedings arising in the normal course of business. As of the date of this report, the Company is not a party to any legal proceeding not described in this section in which an adverse outcome would reasonably be expected to have a material adverse effect on the Company’s results of operations or financial condition. |
Income Taxes
Income Taxes | 6 Months Ended |
Jun. 30, 2015 | |
Income Taxes [Abstract] | |
Income Taxes | (10) Income Taxes The Company is subject to income tax in numerous jurisdictions and at various rates and the use of estimates is required in determining the provision for income taxes. For the six month periods ended June 30, 2015 and 2014, the Company recorded a provision for taxes of $3,179,000 and $3,400,000 on earnings before tax of $9,113,000 and $9,403,000 resulting in an effective income tax rate of 35% and 36%, respectively. The effective tax rates of 35% and 36% for the six month periods ended June 30, 2015 and 2014 consist of a graduated federal rate slightly higher than 34% and state taxes. The Company regularly assesses the likelihood that the deferred tax assets will be recovered from future taxable earnings. The Company considers projected future taxable earnings and ongoing tax planning strategies, and then records a valuation allowance to reduce the carrying value of the net deferred taxes to an amount that is more likely than not to be realized. If the Company’s actual results and updated projections vary significantly from the projections used as a basis for determining its valuation allowance, the Company may need to increase or decrease the valuation allowance against the gross deferred tax assets. The Company will adjust earnings for the deferred tax in the period in which any such determination is made. The Company applies ASC 740, Income Taxes The Company is subject to income tax examinations in the U.S. Federal jurisdiction, as well as in the Republic of Ireland and various state jurisdictions. At June 30, 2015, the Company’s 2013 U.S. Federal 1120 tax filing was under exam by the U.S. Internal Revenue Service. To date no finding or adjustments have been proposed to the Company. At June 30, 2015, tax years 2011 through 2014 remain open to examination. |
Products and Services
Products and Services | 6 Months Ended |
Jun. 30, 2015 | |
Products and Services [Abstract] | |
Products and Services | (11) Products and Services In order to present a more detailed product-specific revenue analysis, beginning in the first quarter of 2015 the Company commenced reporting net revenue for each of its top product lines in each of its primary markets. The following tables set forth, for the periods indicated, net revenue by product line along with the percent change from the previous period for each of the Company’s top eight products by net revenue: Three months ended June 30, 2015 2014 Product Line Primary Market Net Revenue Percent Change Net Revenue (dollars in thousands) GuideLiner ® Interventional cardiology $ 12,272 58 % $ 7,764 Pronto ® Interventional cardiology 3,724 (19 %) 4,622 Vein catheter reprocessing Phlebology 3,048 50 % 2,031 Micro-introducer kits Interventional radiology 2,986 17 % 2,544 Hemostatic patches Interventional cardiology 2,949 (6 %) 3,152 Radial access products Interventional cardiology 1,873 28 % 1,466 Langston ® Interventional cardiology 1,689 37 % 1,229 D-Stat ® Electrophysiology 1,483 7 % 1,389 Six months ended June 30, 2015 2014 Product Line Primary Market Net Revenue Percent Change Net Revenue (dollars in thousands) GuideLiner Interventional cardiology $ 22,612 56 % $ 14,468 Pronto catheters Interventional cardiology 8,106 (13 %) 9,298 Hemostatic patches Interventional cardiology 5,971 (5 %) 6,316 Micro-introducer kits Interventional radiology 5,840 20 % 4,877 Vein catheter reprocessing Phlebology 5,760 22 % 4,711 Radial access products Interventional cardiology 3,511 25 % 2,799 Langston catheters Interventional cardiology 3,268 19 % 2,741 D-Stat Flowable hemostat Electrophysiology 2,855 4 % 2,741 The Company sells its products into four primary clinical markets: interventional cardiology, interventional radiology, electrophysiology, and phlebology (vein treatment). The Company estimates the percentage of its revenue that is generated in each market by estimating the percentage of sales of each product that is made to customers for use in that market. During both the three and six months ended June 30, 2015, the Company estimates that 73% of its product sales by revenue were generated from the interventional cardiology market, 13% from the phlebology market, 10% from the interventional radiology market and 4% from the electrophysiology market. |
Net Earnings per Share (Tables)
Net Earnings per Share (Tables) | 6 Months Ended |
Jun. 30, 2015 | |
Net Earnings per Share [Abstract] | |
Weighted average common shares outstanding | Weighted average common shares outstanding for the three and six months ended June 30, 2015 and 2014 were as follows: Three Months Ended June 30, Six Months Ended June 30, 2015 2014 2015 2014 (unaudited) (unaudited) Weighted average shares outstanding – basic 17,018,000 16,807,000 16,995,000 16,761,000 Weighted average shares outstanding – diluted 17,996,000 17,589,000 17,946,000 17,585,000 |
Inventories (Tables)
Inventories (Tables) | 6 Months Ended |
Jun. 30, 2015 | |
Inventories [Abstract] | |
Inventories | Inventories are comprised of the following: June 30, 2015 December 31, 2014 (dollars in thousands) (unaudited) Raw materials $ 8,761 $ 8,251 Work-in-process 2,039 1,139 Finished goods 9,202 6,518 $ 20,002 $ 15,908 |
Goodwill and Other Intangible21
Goodwill and Other Intangible Assets (Tables) | 6 Months Ended |
Jun. 30, 2015 | |
Goodwill and Other Intangible Assets [Abstract] | |
Goodwill and acquired intangible assets | The changes in the carrying amount of goodwill and acquired intangible assets for the six months ended June 30, 2015 are as follows: Goodwill Acquired Intangibles (dollars in thousands) (unaudited) Balance at December 31, 2014 $ 10,259 $ 10,164 Amortization – (808 ) Foreign currency translation adjustments (178 ) (87 ) Balance at June 30, 2015 $ 10,081 $ 9,269 |
Products and Services (Tables)
Products and Services (Tables) | 6 Months Ended |
Jun. 30, 2015 | |
Products and Services [Abstract] | |
Revenue by product category | The following tables set forth, for the periods indicated, net revenue by product line along with the percent change from the previous period for each of the Company’s top eight products by net revenue: Three months ended June 30, 2015 2014 Product Line Primary Market Net Revenue Percent Change Net Revenue (dollars in thousands) GuideLiner ® Interventional cardiology $ 12,272 58 % $ 7,764 Pronto ® Interventional cardiology 3,724 (19 %) 4,622 Vein catheter reprocessing Phlebology 3,048 50 % 2,031 Micro-introducer kits Interventional radiology 2,986 17 % 2,544 Hemostatic patches Interventional cardiology 2,949 (6 %) 3,152 Radial access products Interventional cardiology 1,873 28 % 1,466 Langston ® Interventional cardiology 1,689 37 % 1,229 D-Stat ® Electrophysiology 1,483 7 % 1,389 Six months ended June 30, 2015 2014 Product Line Primary Market Net Revenue Percent Change Net Revenue (dollars in thousands) GuideLiner Interventional cardiology $ 22,612 56 % $ 14,468 Pronto catheters Interventional cardiology 8,106 (13 %) 9,298 Hemostatic patches Interventional cardiology 5,971 (5 %) 6,316 Micro-introducer kits Interventional radiology 5,840 20 % 4,877 Vein catheter reprocessing Phlebology 5,760 22 % 4,711 Radial access products Interventional cardiology 3,511 25 % 2,799 Langston catheters Interventional cardiology 3,268 19 % 2,741 D-Stat Flowable hemostat Electrophysiology 2,855 4 % 2,741 |
Net Earnings per Share (Details
Net Earnings per Share (Details) - shares | 3 Months Ended | 6 Months Ended | ||
Jun. 30, 2015 | Jun. 30, 2014 | Jun. 30, 2015 | Jun. 30, 2014 | |
Net Earnings per Share [Abstract] | ||||
Weighted average shares outstanding - basic (in shares) | 17,018,000 | 16,807,000 | 16,995,000 | 16,761,000 |
Weighted average shares outstanding - diluted (in shares) | 17,996,000 | 17,589,000 | 17,946,000 | 17,585,000 |
Revenue Recognition (Details)
Revenue Recognition (Details) - 6 months ended Jun. 30, 2015 | Total |
Revenue Recognition [Abstract] | |
Restocking charge (in hundredths) | 20.00% |
Thrombi Pad [Member] | |
Revenue Recognition, Amortization of License Fee [Line Items] | |
Years to amortize license fees | 10 years |
Thrombi Gel [Member] | |
Revenue Recognition, Amortization of License Fee [Line Items] | |
Years to amortize license fees | 10 years |
Thrombi Paste [Member] | |
Revenue Recognition, Amortization of License Fee [Line Items] | |
Years to amortize license fees | 10 years |
Inventories (Details)
Inventories (Details) - USD ($) $ in Thousands | Jun. 30, 2015 | Dec. 31, 2014 |
Inventories [Abstract] | ||
Raw materials | $ 8,761 | $ 8,251 |
Work-in-process | 2,039 | 1,139 |
Finished goods | 9,202 | 6,518 |
Inventory, Total | $ 20,002 | $ 15,908 |
Goodwill and Other Intangible26
Goodwill and Other Intangible Assets (Details) - USD ($) $ in Thousands | 3 Months Ended | 6 Months Ended | ||
Jun. 30, 2015 | Jun. 30, 2014 | Jun. 30, 2015 | Jun. 30, 2014 | |
Goodwill [Abstract] | ||||
Beginning balance | $ 10,259 | |||
Foreign currency translation adjustments | (178) | |||
Ending balance | $ 10,081 | 10,081 | ||
Acquired Intangibles [Abstract] | ||||
Beginning balance | 10,164 | |||
Amortization | (404) | $ (412) | (808) | $ (823) |
Foreign currency translation adjustments | (87) | |||
Ending balance | $ 9,269 | $ 9,269 |
Credit Risk and Allowance for27
Credit Risk and Allowance for Doubtful Accounts (Details) - USD ($) | 6 Months Ended | |
Jun. 30, 2015 | Dec. 31, 2014 | |
Valuation and Qualifying Accounts Disclosure [Line Items] | ||
Number of days outstanding before being considered past due | 60 days | |
Restocking charge (in hundredths) | 20.00% | |
Reserves for accounts receivable, net | $ 420,000 | $ 300,000 |
Allowance for Doubtful Accounts [Member] | ||
Valuation and Qualifying Accounts Disclosure [Line Items] | ||
Reserves for accounts receivable, net | 340,000 | 220,000 |
Sales Return Allowances [Member] | ||
Valuation and Qualifying Accounts Disclosure [Line Items] | ||
Reserves for accounts receivable, net | $ 80,000 | $ 80,000 |
Concentrations of Credit and 28
Concentrations of Credit and Other Risks (Details) | 6 Months Ended | |
Jun. 30, 2015 | Jun. 30, 2014 | |
United States [Member] | ||
Concentration Risk [Line Items] | ||
Concentration risk, percentage (in hundredths) | 77.00% | 83.00% |
International Markets [Member] | ||
Concentration Risk [Line Items] | ||
Concentration risk, percentage (in hundredths) | 23.00% | 17.00% |
Dependence on Key Suppliers (De
Dependence on Key Suppliers (Details) | 6 Months Ended |
Jun. 30, 2015 | |
Kings Pharmaceuticals [Abstract] | |
Initial agreement period | 10 years |
Contract extension period | 1 year |
Period of written notice to supplier | 5 years |
Commitments and Contingencies (
Commitments and Contingencies (Details) - USD ($) | Jul. 28, 2014 | Jun. 30, 2015 | Jun. 30, 2014 | Jun. 30, 2015 | Jun. 30, 2014 | Jul. 31, 2014 |
Governmental Proceedings [Abstract] | ||||||
Product revenue | $ 37,398,000 | $ 30,606,000 | $ 71,839,000 | $ 60,451,000 | ||
Governmental Proceedings [Member] | ||||||
Governmental Proceedings [Abstract] | ||||||
Product revenue | $ 534,000 | |||||
Percentage of sales revenue (in hundredths) | 0.10% | |||||
Alleged damages from product defects to government | $ 20,000,000 | |||||
Payment on settlement of litigation | $ 520,000 |
Income Taxes (Details)
Income Taxes (Details) - USD ($) | 3 Months Ended | 6 Months Ended | |||
Jun. 30, 2015 | Jun. 30, 2014 | Jun. 30, 2015 | Jun. 30, 2014 | Dec. 31, 2014 | |
Income Taxes [Abstract] | |||||
Income tax expense (benefit) | $ 1,935,000 | $ 1,825,000 | $ 3,179,000 | $ 3,400,000 | |
Earnings before income tax | 5,662,000 | $ 5,030,000 | $ 9,113,000 | $ 9,403,000 | |
Effective income tax rate (in hundredths) | 35.00% | 36.00% | |||
Federal statutory income tax rate (in hundredths) | 34.00% | 34.00% | |||
Unrecognized income tax asset | $ 1,262,000 | $ 1,262,000 | $ 1,262,000 | ||
Tax related interest expense | 0 | ||||
Tax related penalties expense | $ 0 |
Products and Services (Details)
Products and Services (Details) $ in Thousands | 3 Months Ended | 6 Months Ended | ||
Jun. 30, 2015USD ($)ProductMarket | Jun. 30, 2014USD ($) | Jun. 30, 2015USD ($)ProductMarket | Jun. 30, 2014USD ($) | |
Product Information [Line Items] | ||||
Number of products | Product | 8 | 8 | ||
Number of primary markets | Market | 4 | 4 | ||
Total revenue | $ 37,550 | $ 30,677 | $ 72,161 | $ 60,584 |
Sales Revenue, Net [Member] | Interventional cardiology [Member] | ||||
Product Information [Line Items] | ||||
Percentage of sales revenue (in hundredths) | 73.00% | 73.00% | ||
Sales Revenue, Net [Member] | Phlebology [Member] | ||||
Product Information [Line Items] | ||||
Percentage of sales revenue (in hundredths) | 13.00% | 13.00% | ||
Sales Revenue, Net [Member] | Interventional radiology [Member] | ||||
Product Information [Line Items] | ||||
Percentage of sales revenue (in hundredths) | 10.00% | 10.00% | ||
Sales Revenue, Net [Member] | Electrophysiology [Member] | ||||
Product Information [Line Items] | ||||
Percentage of sales revenue (in hundredths) | 4.00% | 4.00% | ||
GuideLiner catheters [Member] | ||||
Product Information [Line Items] | ||||
Class of primary market description | Interventional cardiology | |||
Total revenue | $ 12,272 | 7,764 | $ 22,612 | 14,468 |
Total revenue percentage change (in hundredths) | 58.00% | 56.00% | ||
Pronto catheters [Member] | ||||
Product Information [Line Items] | ||||
Class of primary market description | Interventional cardiology | |||
Total revenue | $ 3,724 | 4,622 | $ 8,106 | 9,298 |
Total revenue percentage change (in hundredths) | (19.00%) | (13.00%) | ||
Hemostatic patches [Member] | ||||
Product Information [Line Items] | ||||
Class of primary market description | Interventional cardiology | |||
Total revenue | $ 2,949 | 3,152 | $ 5,971 | 6,316 |
Total revenue percentage change (in hundredths) | (6.00%) | (5.00%) | ||
Micro-introducer kits [Member] | ||||
Product Information [Line Items] | ||||
Class of primary market description | Interventional radiology | |||
Total revenue | $ 2,986 | 2,544 | $ 5,840 | 4,877 |
Total revenue percentage change (in hundredths) | 17.00% | 20.00% | ||
Vein catheter reprocessing [Member] | ||||
Product Information [Line Items] | ||||
Class of primary market description | Phlebology | |||
Total revenue | $ 3,048 | 2,031 | $ 5,760 | 4,711 |
Total revenue percentage change (in hundredths) | 50.00% | 22.00% | ||
Radial access products [Member] | ||||
Product Information [Line Items] | ||||
Class of primary market description | Interventional cardiology | |||
Total revenue | $ 1,873 | 1,466 | $ 3,511 | 2,799 |
Total revenue percentage change (in hundredths) | 28.00% | 25.00% | ||
Langston Catheters [Member] | ||||
Product Information [Line Items] | ||||
Class of primary market description | Interventional cardiology | |||
Total revenue | $ 1,689 | 1,229 | $ 3,268 | 2,741 |
Total revenue percentage change (in hundredths) | 37.00% | 19.00% | ||
D-Stat Flowable hemostat [Member] | ||||
Product Information [Line Items] | ||||
Class of primary market description | Electrophysiology | |||
Total revenue | $ 1,483 | $ 1,389 | $ 2,855 | $ 2,741 |
Total revenue percentage change (in hundredths) | 7.00% | 4.00% |