Westridge Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Westridge Laboratories, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ID Free Personal Lubricant
3
Total
3
Cleared
0
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