Verge Medical, Inc. - FDA 510(k) Cleared Devices
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.
2 devices