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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/aktien/CryoLife-US2289031005">CryoLife</a></div>
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      <a target="_blank" rel="nofollow" href="https://www.prnewswire.com/news-releases/artivion-reports-first-quarter-2026-financial-results-and-announces-exercise-of-option-to-acquire-endospan-302766107.html">Artivion Reports First Quarter 2026 Financial Results and Announces Exercise of Option to Acquire Endospan</a>
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        First Quarter &amp; Recent Business Highlights: Achieved revenue of $116.3 million in the first quarter of 2026 versus $99.0 million in the first quarter of 2025, an increase of 18% on a GAAP basis and 12% on a non-GAAP constant currency basis  Net income for the first quarter of 2026 was $1.4 million, or $0.03 per fully diluted share, and non-GAAP net income was $4.2 million, or $0.08 per fully di...
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      <a target="_blank" rel="nofollow" href="https://www.prnewswire.com/news-releases/artivion-announces-release-date-and-teleconference-call-details-for-first-quarter-2026-financial-results-302752177.html">Artivion Announces Release Date and Teleconference Call Details for First Quarter 2026 Financial Results</a>
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        ATLANTA, April 23, 2026 /PRNewswire/ -- Artivion, Inc. (NYSE: AORT), a leading cardiac and vascular surgery company focused on aortic disease, announced today that first quarter 2026 financial results will be released on Thursday, May 7, 2026, after the market closes. On that day, the Company will hold a teleconference call and live webcast at 4:30 p.m.
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      <a target="_blank" rel="nofollow" href="https://www.prnewswire.com/news-releases/artivion-announces-us-fda-approval-of-the-nexus-aortic-arch-system-302735203.html">Artivion Announces U.S. FDA Approval of the NEXUS® Aortic Arch System</a>
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        Endospan&#39;s NEXUS branched endovascular stent graft system shown to effectively treat aortic arch disease, including chronic aortic dissections ATLANTA, April 7, 2026 /PRNewswire/ -- Artivion, Inc. (NYSE: AORT), a leading cardiac and vascular surgery company focused on aortic disease, today announced that the U.S. Food and Drug Administration (FDA) has approved the premarket approval application...
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