Medical Device Manufacturer · US , Crofton , MD

Westridge Laboratories, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2006

Total

Cleared

Denied

Westridge Laboratories, Inc. has 3 FDA 510(k) cleared medical devices. Based in Crofton, US.

Latest FDA clearance: Sep 2024. Active since 2006. Primary specialty: Obstetrics & Gynecology.

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

510(k) submissions have been managed by Erica Loring as regulatory consultant.

FDA 510(k) Regulatory Record - Westridge Laboratories, Inc.

3 devices

1-3 of 3

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: May 11, 2026