Verge Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Verge Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: FLASH Flex™ Aorto-Ostial Angioplasty System, RoVo Mechanical Thrombectomy System
2
Total
2
Cleared
0
Denied
Verge Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Campbell, US.
Latest FDA clearance: Apr 2026. Active since 2026. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Verge Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Bridge City Regulatory, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Verge Medical, Inc.
2 devices