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.

FDA 510(k) cleared devices by Westridge Laboratories, Inc.

3 devices

1-3 of 3