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Artivion Secures US FDA Approval for Endospan's NEXUS Aortic Arch System
Artivion, Inc., a leading cardiac and vascular surgery company focused on aortic disease, announced that the US Food and Drug Administration (FDA) has approved the premarket approval application (PMA) for the NEXUS Aortic Arch System, developed by Endospan Ltd. (Endospan), Artivion's long-standing partner.
NEXUS Aortic Arch System | 08/04/2026 | By Darshana
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