8-K

ARTIVION, INC. (AORT)

8-K 2023-08-03 For: 2023-08-03
View Original
Added on April 10, 2026

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

WASHINGTON, D.C. 20549

___________________________________________

FORM 8-K

___________________________________________

CURRENT REPORT

PURSUANT TO SECTION 13 OR 15(d) OF THE

SECURITIES EXCHANGE ACT OF 1934

Date of Report (Date of earliest event reported): August 3, 2023

___________________________________________

ARTIVION, INC.

(Exact name of registrant as specified in its charter)

___________________________________________

Delaware 1-13165 59-2417093
(State or Other Jurisdiction<br>of Incorporation) (Commission File Number) (IRS Employer<br><br>Identification No.)

1655 Roberts Boulevard, N.W., Kennesaw, Georgia 30144

(Address of principal executive office) (zip code)

Registrant's telephone number, including area code: (770) 419-3355

___________________________________________________________________________________

(Former name or former address, if changed since last report)

Title of each class Trading Symbol(s) Name of each exchange <br>on which registered
Common Stock, $0.01 par value AORT NYSE

___________________________________________

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions (see General Instruction A.2. below):

Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).

Emerging growth company ☐

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐

Item 2.02    Results of Operations and Financial Condition

On August 3, 2023, Artivion, Inc. (“Artivion”) issued a press release announcing its financial results for the second quarter ended June 30, 2023. Artivion hereby incorporates by reference herein the information set forth in its press release dated August 3, 2023, a copy of which is attached hereto as Exhibit 99.1. Except as otherwise provided in the press release, the press release speaks only as of the date of such press release and it shall not create any implication that the affairs of Artivion have continued unchanged since such date.

The information provided pursuant to this Item 2.02 is to be considered “furnished” pursuant to Item 2.02 of Form 8-K and shall not be deemed to be “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended, or otherwise subject to the liabilities of that Section or Sections 11 and 12(a)(2) of the Securities Act of 1933, as amended, nor shall it be deemed incorporated by reference into any of Artivion’s reports or filings with the Securities and Exchange Commission, whether made before or after the date hereof, except as expressly set forth by specific reference in such report or filing.

Except for the historical information contained in this report, the statements made by Artivion are forward-looking statements that involve risks and uncertainties. All such statements are subject to the safe harbor created by the Private Securities Litigation Reform Act of 1995. Artivion’s future financial performance could differ significantly from the expectations of management and from results expressed or implied in the press release.  Please refer to the last paragraph of the text portion of the press release for further discussion about forward-looking statements. For further information on risk factors, please refer to “Risk Factors” contained in Artivion’s most recently filed Form 10-K and its subsequent filings with the Securities and Exchange Commission, as well as in the press release attached as Exhibit 99.1 hereto. Artivion disclaims any obligation or duty to update or modify these forward-looking statements.

Item 9.01(d)    Exhibits

(d)Exhibits.

Exhibit Number Description
99.1* Press Release dated August 3, 2023.
104 Cover Page Interactive Data File (formatted as Inline XBRL and contained in Exhibit 101).

*Furnished herewith, not filed.

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SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, Artivion, Inc. has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

Date: August 3, 2023

ARTIVION, INC.
By: /s/ D. Ashley Lee
Name: D. Ashley Lee
Title: Executive Vice President and<br><br>Chief Financial Officer

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Document

Exhibit 99.1

aort_logoa.jpg

FOR IMMEDIATE RELEASE

Contacts:

Artivion Gilmartin Group LLC
D. Ashley Lee Brian Johnston / Lynn Lewis
Executive Vice President & Phone: 332-895-3222
Chief Financial Officer investors@artivion.com
Phone: 770-419-3355

Artivion Reports Second Quarter 2023 Financial Results

Second Quarter and Recent Business Highlights:

•Achieved revenue of $89.3 million in the second quarter of 2023 versus $80.3 million in the second quarter of 2022, an increase of 11% on both a GAAP and non-GAAP constant currency basis

•Net loss was ($3.4) million or ($0.08) per share; non-GAAP net income was $2.3 million or $0.06 per share

•Achieved EBITDA of $9.2 million in the second quarter of 2023; non-GAAP adjusted EBITDA increased 35% to $13.8 million in the second quarter of 2023 compared to the second quarter of 2022

•Aortic stent graft revenues increased 19% on both a GAAP and non-GAAP constant currency basis in the second quarter of 2023 compared to the second quarter of 2022

•On-X revenues increased 10% on a GAAP basis and 11% on a non-GAAP constant currency basis in the second quarter of 2023 compared to the second quarter of 2022

•Received PerClot PMA approval and commenced shipping product to Baxter

•Patient enrollment in the PERSEVERE clinical trial accelerated with enrollment completion expected in the third quarter of 2023

ATLANTA, GA – (August 3, 2023) – Artivion, Inc. (NYSE: AORT), a leading cardiac and vascular surgery company focused on aortic disease, today announced its financial results for the second quarter ended June 30, 2023.

“Our second quarter results reflect the strength of our business commercially, operationally, and financially. We delivered double-digit constant currency revenue growth year-over-year for the second consecutive quarter and remain on track to achieve or exceed the revenue and EBITDA growth targets for this year. Our exceptional second quarter performance was driven by year-over-year aortic stent graft revenue growth of 19%, On-X revenue growth of 10%, tissue processing growth of 9%, and BioGlue growth of 4%. On a constant currency basis, year-over-year aortic stent graft, On-X, tissue processing, and BioGlue revenue growth were 19%, 11%, 9%, and 4%, respectively. We also saw Asia Pacific and Latin American revenue grow 23% and 21%, respectively, and 23% and 24% on a constant currency basis, compared to last year,” said Pat Mackin, Chairman, President, and Chief Executive Officer.

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Mr. Mackin added, “In addition to our strong commercial results, we also obtained FDA approval for PerClot and, accordingly, received the net $14.3 million FDA approval milestone payment from Baxter. Immediately thereafter, we also began shipping PerClot to Baxter, pursuant to the terms of our agreement. Further, we had strong revenue growth in our aortic stent graft product line, driven by accelerating productivity levels at our German manufacturing facility. We improved patient enrollment for our PERSEVERE trial evaluating AMDS, a simple, elegant stent graft solution to treat aortic arch disease, and we still anticipate completing enrollment in that trial in the third quarter of this year.

Mr. Mackin concluded, “Given our solid execution in the first half of 2023 and strong business momentum, we are now on a path to meet or exceed our current year guidance, as well as to achieve our 2024 commitments to deliver double-digit compounded annual constant currency revenue growth and adjusted EBITDA in excess of $75.0 million.”

Second Quarter 2023 Financial Results

Total revenues for the second quarter of 2023 were $89.3 million, an increase of 11% on both a GAAP and non-GAAP constant currency basis, both compared to the second quarter of 2022.

Net loss for the second quarter of 2023 was ($3.4) million, or ($0.08) per fully diluted common share, compared to net loss of ($4.3) million, or ($0.11) per fully diluted common share for the second quarter of 2022. Net loss for the second quarter of 2023 includes pretax charges of $10.9 million related to contingent consideration for the acquisition of AMDS and $5.0 million related to the final payment to Endospan under our September 2019 Loan Agreement with Endospan, partially offset by a net pretax gain of $14.3 million related to the PerClot PMA approval milestone net payment. Non-GAAP net income for the second quarter of 2023 was $2.3 million, or $0.06 per fully diluted common share, compared to non-GAAP net loss of ($1.3) million, or ($0.03) per fully diluted common share for the second quarter of 2022.

2023 Financial Outlook

Artivion is raising its revenue guidance range and now expects to achieve constant currency revenue growth of between 10% and 12%, compared to the previous range of 9% and 12%, for the full year 2023 compared to 2022. The Company expects revenues to be in a range of $342.0 million and $350.0 million, compared to the previous range of $337.0 million and $348.0 million.

Additionally, Artivion continues to expect adjusted EBITDA, as reported, to increase greater than 25% in 2023 compared to 2022, resulting in adjusted EBITDA in excess of $52.0 million for 2023.

The Company's financial performance for 2023 and future periods is subject to the risks identified below.

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Non-GAAP Financial Measures

This press release contains non-GAAP financial measures, including non-GAAP revenue, non-GAAP net income, non-GAAP EBITDA, and non-GAAP general, administrative, and marketing expenses. Investors should consider this non-GAAP information in addition to, and not as a substitute for, financial measures prepared in accordance with US GAAP. In addition, this non-GAAP financial information may not be the same as similar measures presented by other companies. The Company's non-GAAP revenues are adjusted for the impact of changes in currency exchange. The Company’s non-GAAP net income; non-GAAP EBITDA; and non-GAAP general, administrative, and marketing results exclude (as applicable) depreciation and amortization expense; interest income and expense; stock-based compensation expense; loss or gain on foreign currency revaluation; income tax expense or benefit; corporate rebranding expense; business development, integration, and severance income or expense; non-cash interest expense; gain from sale of non-financial assets, and abandonment of CardioGenesis cardiac laser therapy business. The Company generally uses non-GAAP financial measures to facilitate management's review of the operational performance of the company and as a basis for strategic planning. Company management believes that these non-GAAP presentations provide useful information to investors regarding unusual non-operating transactions; the operating expense structure of the Company's existing and recently acquired operations, without regard to its on-going efforts to acquire additional complementary products and businesses, and the transaction and integration expenses incurred in connection with recently acquired and divested product lines; and the operating expense structure excluding fluctuations resulting from foreign currency revaluation and stock-based compensation expense. The Company believes it is useful to exclude certain expenses because such amounts in any specific period may not directly correlate to the underlying performance of its business operations or can vary significantly between periods as a result of factors such as impact of recent acquisitions, non-cash expense related to amortization of previously acquired tangible and intangible assets, and any related adjustments to their carrying values. The Company has adjusted for the impact of changes in currency exchange from certain revenues to evaluate comparable product growth rates on a constant currency basis. The Company does, however, expect to incur similar types of expenses and currency exchange impacts in the future, and this non-GAAP financial information should not be viewed as a statement or indication that these types of expenses will not recur. Company management encourages investors to review the Company's consolidated financial statements and publicly filed reports in their entirety, including the reconciliation of GAAP to non-GAAP financial measures.”

Webcast and Conference Call Information

The Company will hold a teleconference call and live webcast later today, August 3, 2023, at 4:30 p.m. ET to discuss the results, followed by a question and answer session. To participate in the conference call dial 201-689-8261 a few minutes prior to 4:30 p.m. ET. The teleconference replay will be available approximately one hour following the completion of the event and can be accessed by calling (toll free) 877-660-6853 or 201-612-7415. The conference number for the replay is 13739398.

The live webcast and replay can be accessed by going to the Investors section of the Artivion website at www.Artivion.com and selecting the heading Webcasts & Presentations.

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About Artivion, Inc.

Headquartered in suburban Atlanta, Georgia, Artivion, Inc. is a medical device company focused on developing simple, elegant solutions that address cardiac and vascular surgeons’ most difficult challenges in treating patients with aortic diseases. Artivion’s four major groups of products include: aortic stent grafts, surgical sealants, On-X mechanical heart valves, and implantable cardiac and vascular human tissues. Artivion markets and sells products in more than 100 countries worldwide. For additional information about Artivion, visit our website, www.artivion.com.

Forward Looking Statements

Statements made in this press release that look forward in time or that express management's beliefs, expectations, or hopes are forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Such forward-looking statements reflect the views of management at the time such statements are made. These statements include our beliefs that we remain on track to achieve or exceed the revenue and EBITDA growth targets for this year; and we are now on a path to meet or exceed our current year guidance, as well as to achieve our 2024 commitments to deliver double-digit compounded annual constant currency revenue growth and adjusted EBITDA in excess of $75.0 million. These forward-looking statements are subject to a number of risks, uncertainties, estimates, and assumptions that may cause actual results to differ materially from current expectations, including that the benefits anticipated from the Ascyrus Medical LLC transaction and Endospan agreements may not be achieved at all or at the levels we had originally anticipated; the benefits anticipated from our clinical trials may not be achieved or achieved on our anticipated timeline; our products may not be able to consistently retain their existing regulatory approvals or special regulatory approvals in order to be commercialized; products in our pipeline may not receive regulatory approval at all or receive regulatory approval on our anticipated timelines; or our products that obtain regulatory approval may not be adopted by the market as much as we anticipate or at all. These risks and uncertainties include the risk factors detailed in our Securities and Exchange Commission filings, including our Form 10-K for the year ended December 31, 2022 and our Form 10-Q for the quarter ended June 31, 2023. Artivion does not undertake to update its forward-looking statements, whether as a result of new information, future events, or otherwise.

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Artivion, Inc. and Subsidiaries

Condensed Consolidated Statements of Operations and Comprehensive Loss

In Thousands, Except Per Share Data

(Unaudited)

Three Months Ended<br>June 30, Six Months Ended<br>June 30,
2023 2022 2023 2022
Revenues:
Products $ 66,003 $ 58,936 $ 128,294 $ 116,478
Preservation services 23,248 21,404 44,186 41,075
Total revenues 89,251 80,340 172,480 157,553
Cost of products and preservation services:
Products 20,977 18,230 40,510 35,638
Preservation services 10,190 9,938 20,159 19,024
Total cost of products and preservation services 31,167 28,168 60,669 54,662
Gross margin 58,084 52,172 111,811 102,891
Operating expenses:
General, administrative, and marketing 57,241 38,983 107,606 77,938
Research and development 7,418 8,648 14,641 18,776
Total operating expenses 64,659 47,631 122,247 96,714
Gain from sale of non-financial assets (14,250) (14,250)
Operating income 7,675 4,541 3,814 6,177
Interest expense 6,356 4,101 12,452 8,049
Interest income (265) (30) (340) (46)
Other expense, net 4,241 3,770 3,278 3,903
Loss before income taxes (2,657) (3,300) (11,576) (5,729)
Income tax expense 725 959 5,338 1,919
Net loss $ (3,382) $ (4,259) $ (16,914) $ (7,648)
Loss per share:
Basic $ (0.08) $ (0.11) $ (0.41) $ (0.19)
Diluted $ (0.08) $ (0.11) $ (0.41) $ (0.19)
Weighted-average common shares outstanding:
Basic 40,755 40,031 40,595 39,941
Diluted 40,755 40,031 40,595 39,941
Net loss $ (3,382) $ (4,259) $ (16,914) $ (7,648)
Other comprehensive loss:
Foreign currency translation adjustments 1,826 (14,796) 5,442 (18,571)
Comprehensive loss $ (1,556) $ (19,055) $ (11,472) $ (26,219)

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Artivion, Inc. and Subsidiaries

Condensed Consolidated Balance Sheets

In Thousands

June 30,<br>2023 December 31,<br>2022
(Unaudited)
ASSETS
Current assets:
Cash and cash equivalents $ 48,775 $ 39,351
Trade receivables, net 64,806 61,820
Other receivables 4,450 7,764
Inventories, net 78,458 74,478
Deferred preservation costs, net 48,302 46,371
Prepaid expenses and other 19,107 17,550
Total current assets 263,898 247,334
Goodwill 245,561 243,631
Acquired technology, net 147,029 151,263
Operating lease right-of-use assets, net 40,825 41,859
Property and equipment, net 38,389 38,674
Other intangibles, net 29,966 31,384
Deferred income taxes 3,951 1,314
Other assets 8,242 7,339
Total assets $ 777,861 $ 762,798
LIABILITIES AND SHAREHOLDERS' EQUITY
Current liabilities:
Accounts payable $ 10,455 $ 12,004
Accrued expenses 10,365 12,374
Accrued compensation 12,792 13,810
Taxes payable 10,641 2,635
Current maturities of operating leases 4,037 3,308
Accrued procurement fees 1,744 2,111
Current portion of long-term debt 1,561 1,608
Other liabilities 4,635 1,825
Total current liabilities 56,230 49,675
Long-term debt 306,109 306,499
Contingent consideration 56,100 40,400
Non-current maturities of operating leases 39,989 41,257
Deferred income taxes 19,469 24,499
Deferred compensation liability 6,541 5,468
Non-current finance lease obligation 3,446 3,644
Other liabilities 7,469 7,027
Total liabilities $ 495,353 $ 478,469
Commitments and contingencies
Shareholders' equity:
Preferred stock
Common stock (75,000 shares authorized, 42,443 and 41,830 shares issued and outstanding in 2023 and 2022, respectively) 424 418
Additional paid-in capital 347,030 337,385
Retained deficit (34,131) (17,217)
Accumulated other comprehensive loss (16,167) (21,609)
Treasury stock, at cost, 1,487 shares as of June 30, 2023 and December 31, 2022 (14,648) (14,648)
Total shareholders' equity 282,508 284,329
Total liabilities and shareholders' equity $ 777,861 $ 762,798

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Artivion, Inc. and Subsidiaries

Condensed Consolidated Statement of Cash Flows

In Thousands

(Unaudited)

Six Months Ended<br>June 30,
2023 2022
Net cash flows from operating activities:
Net loss $ (16,914) $ (7,648)
Adjustments to reconcile net loss to net cash from operating activities:
Change in fair value of contingent consideration 15,700 (5,000)
Depreciation and amortization 11,501 11,497
Non-cash compensation 7,279 6,100
Fair value adjustment of long-term loan 5,000
Non-cash lease expense 3,631 3,803
Write-down of inventories and deferred preservation costs 2,021 2,177
Deferred income taxes (8,073) (1,611)
Gain from sale of non-financial assets (14,250)
Other 1,836 940
Changes in operating assets and liabilities:
Accounts payable, accrued expenses, and other liabilities 1,607 (5,677)
Receivables 655 (9,635)
Prepaid expenses and other assets (2,317) (205)
Inventories and deferred preservation costs (6,921) (3,653)
Net cash flows provided by (used in) operating activities 755 (8,912)
Net cash flows from investing activities:
Proceeds from sale of non-financial assets, net 14,250
Capital expenditures (4,029) (4,055)
Payments for Endospan Agreement (5,000)
Other (986) (939)
Net cash flows provided by (used in) investing activities 4,235 (4,994)
Net cash flows from financing activities:
Proceeds from financing insurance premiums 3,558
Proceeds from exercise of stock options and issuance of common stock 2,581 2,318
Principal payments on short-term notes payable (529)
Redemption and repurchase of stock to cover tax withholdings (563) (1,739)
Repayment of term loan (1,381) (1,370)
Other (262) (241)
Net cash flows provided by (used in) financing activities 3,404 (1,032)
Effect of exchange rate changes on cash and cash equivalents 1,030 310
Increase (decrease) in cash and cash equivalents 9,424 (14,628)
Cash and cash equivalents beginning of period 39,351 55,010
Cash and cash equivalents end of period $ 48,775 $ 40,382

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Artivion, Inc. and Subsidiaries

Financial Highlights

In Thousands

(Unaudited)

Three Months Ended<br>June 30, Six Months Ended<br>June 30,
2023 2022 2023 2022
Products:
Aortic stent grafts $ 28,359 $ 23,833 $ 54,509 $ 49,339
On-X 17,946 16,255 35,602 30,626
Surgical sealants 16,566 15,967 33,269 31,648
Other 3,132 2,881 4,914 4,865
Total products 66,003 58,936 128,294 116,478
Preservation services 23,248 21,404 44,186 41,075
Total revenues $ 89,251 $ 80,340 $ 172,480 $ 157,553
Revenues:
US $ 44,425 $ 40,953 $ 85,758 $ 78,688
International 44,826 39,387 $ 86,722 78,865
Total revenues $ 89,251 $ 80,340 $ 172,480 $ 157,553

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Artivion, Inc. and Subsidiaries

Reconciliation of GAAP to Non-GAAP

Revenues and General, Administrative, and Marketing Expense

In Thousands

(Unaudited)

Revenues for the<br>Three Months Ended<br>June 30, Percent<br>Change<br>From Prior<br>Year
2023 2022
US GAAP US GAAP Exchange rate effect Constant Currency Constant Currency
Products:
Aortic stent grafts $ 28,359 $ 23,833 29 $ 23,862 19%
On-X 17,946 16,255 (72) 16,183 11%
Surgical sealants 16,566 15,967 (69) 15,898 4%
Other 3,132 2,881 (4) 2,877 9%
Total products 66,003 58,936 (116) 58,820 12%
Preservation services 23,248 21,404 (34) 21,370 9%
Total $ 89,251 $ 80,340 $ (150) $ 80,190 11% Revenues for the<br>Six Months Ended<br>June 30, Percent<br>Change<br>From Prior<br>Year
--- --- --- --- --- --- --- --- --- ---
2023 2022
US GAAP US GAAP Exchange rate effect Constant Currency Constant Currency
Products:
Aortic stent grafts $ 54,509 $ 49,339 (1,209) $ 48,130 13%
On-X 35,602 30,626 (219) 30,407 17%
Surgical sealants 33,269 31,648 (354) 31,294 6%
Other 4,914 4,865 (19) 4,846 1%
Total products 128,294 116,478 (1,801) 114,677 12%
Preservation services 44,186 41,075 (69) 41,006 8%
Total $ 172,480 $ 157,553 $ (1,870) $ 155,683 11% Three Months Ended<br>June 30, Six Months Ended<br>June 30,
--- --- --- --- --- --- --- --- ---
2023 2022 2023 2022
Reconciliation of G&A expense, GAAP to adjusted G&A, non-GAAP:
General, administrative, and marketing expense, GAAP $ 57,241 $ 38,983 $ 107,606 $ 77,938
Business development, integration, and severance expense (income) 11,101 (3,101) 16,098 (4,680)
Corporate rebranding expense 69 289 218 1,172
Abandonment of CardioGenesis cardiac laser therapy business 160 160
Adjusted G&A, non-GAAP $ 45,911 $ 41,795 $ 91,130 $ 81,446

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Artivion, Inc. and Subsidiaries

Reconciliation of GAAP to Non-GAAP

Adjusted EBITDA

In Thousands

(Unaudited)

Three Months Ended<br>June 30, Six Months Ended<br>June 30,
2023 2022 2023 2022
Reconciliation of net loss, GAAP to adjusted EBITDA, non-GAAP:
Net loss, GAAP $ (3,382) $ (4,259) $ (16,914) $ (7,648)
Adjustments:
Business development, integration, and severance expense (income) 15,270 (3,101) 20,722 (4,680)
Interest expense 6,356 4,101 12,452 8,049
Depreciation and amortization expense 5,767 5,616 11,501 11,497
Stock-based compensation expense 3,938 2,934 7,279 6,100
Income tax expense 725 959 5,338 1,919
Abandonment of CardioGenesis cardiac laser therapy business 390 390
Corporate rebranding expense 69 289 218 1,172
Interest income (265) (30) (340) (46)
(Gain) loss on foreign currency revaluation (797) 3,754 (1,770) 3,887
Gain from sale of non-financial assets (14,250) (14,250)
Adjusted EBITDA, non-GAAP $ 13,821 $ 10,263 $ 24,626 $ 20,250

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Artivion Inc. and Subsidiaries

Reconciliation of GAAP to Non-GAAP

Net Income and Diluted Income Per Common Share

In Thousands, Except Per Share Data

(Unaudited)

Three Months Ended<br>June 30, Six Months Ended<br>June 30,
2023 2022 2023 2022
GAAP:
Loss before income taxes $ (2,657) $ (3,300) $ (11,576) $ (5,729)
Income tax expense 725 959 5,338 1,919
Net loss $ (3,382) $ (4,259) $ (16,914) $ (7,648)
Diluted loss per common share $ (0.08) $ (0.11) $ (0.41) $ (0.19)
Diluted weighted-average common shares outstanding 40,755 40,031 40,595 39,941
Reconciliation of loss before income taxes, GAAP to adjusted income (loss), non-GAAP:
Loss before income taxes, GAAP: $ (2,657) $ (3,300) $ (11,576) $ (5,729)
Adjustments:
Business development, integration, and severance expense (income) 15,270 (3,101) 20,722 (4,680)
Amortization expense 3,806 3,905 7,687 7,989
Non-cash interest expense 464 457 926 913
Abandonment of CardioGenesis cardiac laser therapy business 390 390
Corporate rebranding expense 69 289 218 1,172
Gain from sale of non-financial assets (14,250) (14,250)
Adjusted income (loss) before income taxes, non-GAAP 3,092 (1,750) 4,117 (335)
Income tax expense (benefit) calculated at a tax rate of 25% 773 (438) 1,029 (84)
Adjusted net income (loss), non-GAAP $ 2,319 $ (1,312) $ 3,088 $ (251)
Reconciliation of diluted loss per common share, GAAP to adjusted diluted income (loss) per common share, non-GAAP:
Diluted loss per common share, GAAP: $ (0.08) $ (0.11) $ (0.41) $ (0.19)
Adjustments:
Business development, integration, and severance expense (income) 0.37 (0.08) 0.50 (0.12)
Effect of 25% tax rate 0.03 0.05 0.20 0.08
Amortization expense 0.09 0.10 0.19 0.20
Non-cash interest expense 0.01 0.01 0.02 0.02
Abandonment of CardioGenesis cardiac laser therapy business 0.01 0.01
Corporate rebranding expense 0.01 0.01 0.03
Tax effect of non-GAAP adjustments (0.03) (0.01) (0.10) (0.03)
Gain from sale of non-financial assets (0.34) (0.34)
Adjusted diluted income (loss) per common share, non-GAAP $ 0.06 $ (0.03) $ 0.08 $ (0.01)
Reconciliation of diluted weighted-average common shares outstanding GAAP to diluted weighted-average common shares outstanding, non-GAAP:
Diluted weighted-average common shares outstanding, GAAP: 40,755 40,031 40,595 39,941
Adjustments:
Effect of dilutive stock options and awards 419 444
Diluted weighted-average common shares outstanding, non-GAAP 41,174 40,031 41,039 39,941

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