JenaValve Technology Inc has raised $100.4M in total funding. The most recent round was Series C.
JenaValve Technology Inc is headquartered in Irvine, CA.
High-risk patients with severe, symptomatic aortic regurgitation (AR) previously had no FDA-approved transcatheter (minimally invasive) heart valve treatment option, since a transcatheter solution for AR had been considered impossible.
JenaValve's Trilogy Transcatheter Heart Valve System is an FDA-approved TAVR device for aortic regurgitation, using locator technology and a self-expanding nitinol frame to attach securely to native valve leaflets and a purpose-built delivery/introducer system for precise deployment.
The page states Trilogy is 'the only TAVR system FDA-approved for aortic regurgitation,' with locator technology that anchors to native leaflets even without calcium, and cites pivotal study data showing 95% technical success and 1.3% valve embolization versus 74-86% success and >12% embolization for off-label TAVR devices.
JenaValve's investors include Bain Capital Life Sciences and the Qatar Investment Authority.
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