Edwards Lifesciences' INSPIRIS RESILIA Valve Wins FDA Nod

 | Jul 06, 2017 05:45AM ET

Global major in patient-focused innovation for structural heart disease and critical care monitoring, Edwards Lifesciences Corporation (NYSE:EW) is making constant efforts to expand its Surgical Heart Valve Therapy business. The company recently announced the receipt of FDA approval for its INSPIRIS RESILIA aortic valve.

The approval came on the heels of favorable data from the COMMENCE pivotal trial. Per the study, two-year data on 689 patients showed no cases of structural valve deterioration, valve thrombosis or nonstructural valve dysfunction.

INSPIRIS RESILIA aortic valve is a first-of-its-kind resilient heart valve. The valve contains a breakthrough tissue technology that delivers the combination of enhanced anti-calcification properties, improved sustained hemodynamic performance and dry storagenamed RESILIA tissue.

Another feature which lends an edge to the INSPIRIS valve is its VFit technology. The technology incorporates fluoroscopically visible size markers and is designed for potential valve-in-valve procedures. Also, the INSPIRIS valve is a trusted valve platform which is built on the proven performance of the Carpentier-Edwards PERIMOUNT valve design.

The valve is expected to be launched in the U.S. in early 2018. According to Research and Markets, the Global Heart Valve Devices Market is expected to see a CAGR of 13.35% during 2016-2021.