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.

Venclose, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

4 devices

1-4 of 4