Medical Device Manufacturer · US , Newport Beach , CA

Ventris Medical - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2022

Total

Cleared

Denied

Ventris Medical has 5 FDA 510(k) cleared medical devices. Based in Newport Beach, US.

Latest FDA clearance: Jul 2026. Active since 2022. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Ventris Medical Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Bruder Consulting & Venture Group and Trisler Consulting, Dba.

Ventris Medical is one of 16283 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Ventris Medical

5 devices

1-5 of 5

Data Source

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

Last updated: Aug 06, 2026