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Artivion Announces Treatment of First Patient with Arcevo LSA in ARTIZEN Pivotal Trial

Provided By PR Newswire

Last update: Nov 6, 2025

ATLANTA, Nov. 6, 2025 /PRNewswire/ -- Artivion, Inc. (NYSE: AORT), a leading cardiac and vascular surgery company focused on aortic disease, today announced the treatment of the first patient in the ARTIZEN pivotal trial, evaluating the safety and effectiveness of the Arcevo™ LSA Hybrid Stent Graft System ("Arcevo LSA") in the treatment of acute and chronic arch pathologies. The trial is designed to support the Company's forthcoming application to the U.S. Food and Drug Administration (FDA) for Premarket Approval (PMA) of Arcevo LSA.

Read more at prnewswire.com

ARTIVION INC

NYSE:AORT (11/17/2025, 8:04:00 PM)

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