Medical Device Manufacturer · US , Minneapolis , MN

Mentor Urology, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1997

Total

Cleared

Denied

Mentor Urology, Inc. has 1 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Historical record: 1 cleared submissions from 1997 to 1997. Primary specialty: Gastroenterology & Urology.

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

FDA 510(k) cleared devices by Mentor Urology, Inc.

1 devices

1-1 of 1

Data Source

Sourced from the FDA 510(k) public files . 174,477 total devices indexed.

Last updated: Mar 22, 2026