Medical Device Manufacturer · US , Portland , ME

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

5 submissions · 5 cleared · Since 1992

Total

Cleared

Denied

Ventrex, Inc. has 5 FDA 510(k) cleared medical devices. Based in Portland, US.

Historical record: 5 cleared submissions from 1992 to 2006. Primary specialty: Obstetrics & Gynecology.

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

FDA 510(k) cleared devices by Ventrex, Inc.

5 devices

1-5 of 5