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.

510(k) submissions have been managed by Pamela M. Buckman, Msn as regulatory consultant.

Venclose, Inc. is one of 16362 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

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Apr 27, 2026