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enVVeno Receives Unfavorable Appeal Decision from the FDA for the VenoValve
IRVINE, CA / ACCESS Newswire / November 13, 2025 / enVVeno Medical Corporation (NASDAQ:NVNO) ("enVVeno" or the "Company"), a company setting new standards of care for the treatment of deep venous disease, today announced that it has received an unfavorable ...
About this update from Envveno Medical Corporation
[{"type":"text","content":"IRVINE, CA / ACCESS Newswire / November 13, 2025 / enVVeno Medical Corporation (NASDAQ:NVNO) ("enVVeno" or the "Company"), a company setting new standards of care for the treatment of deep venous disease, today announced that it has received an unfavorable decision from the U.S. Food & Drug Administration ("FDA") in response to its supervisory appeal of the not-approvable letter it received on August 19, 2025 in response to its Premarket Approval (PMA) application for VenoValve®, a surgical replacement venous valve for treating severe deep chronic venous insufficiency (CVI). The supervisory appeal upheld the review staff decision in the not-approvable letter that the VenoValve did not meet the standard of reasonable assurance of safety and effectiveness.","length":798,"tagName":"p"},{"type":"image","alt":"","displaySize":"","headline":null,"caption":"","credit":null,"className":"","disableSlideshowImg":false,"size":{"original":{"width":278,"height":85,"url":"https://media.zenfs.com/en/accesswire.ca/a520fbadde0ccf2c97459e37cd95bbd9"},"resized":{"url":"https://s.yimg.com/ny/api/res/1.2/UY2GT6Q7vnYaZ8yxXQOoGQ--/YXBwaWQ9aGlnaGxhbmRlcjt3PTQyMDtoPTEyODtjZj13ZWJw/https://media.zenfs.com/en/accesswire.ca/a520fbadde0ccf2c97459e37cd95bbd9","width":278,"height":85}},"href":"https://app.accessnewswire.com/imagelibrary/71f130b3-017b-4a4e-9360-4cc7bf07b88b/1102264/envveno0logo0-972125.jpg","hrefExternal":true,"rel":"nofollow"},{"type":"text","content":""Although the appeal decision was not the result we are looking for, it did provide valuable insight into the criteria that would be necessary for approval of enVVe, our next generation transcatheter based replacement venous valve," said Robert Berman, enVVeno Medical's Chief Executive Officer. "enVVe should have a different safety profile than an open surgical device and is ready for human testing. Assuming that we can reach alignment with the Agency on achieveble endpoints for enVVe, it makes sense to turn our attention and devote our resources to enVVe. We will continue to interact with the FDA on enVVe and will provide periodic updates on our progress."","length":689,"tagName":"p"},{"type":"text","content":"The Company reported $31.5 million in cash and investments at the end of the third quarter. With its quarterly cash burn of $4 t...