Medical Device Manufacturer · US , San Jose , CA

Venclose, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2016

Total

Cleared

Denied

Venclose, Inc. has 4 FDA 510(k) cleared medical devices. Based in San Jose, US.

Latest FDA clearance: Aug 2025. Active since 2016. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Venclose, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Venclose, Inc.

4 devices

1-4 of 4