Goodmark USA, Inc. is one of 25253 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Goodmark USA, Inc. - FDA 510(k) Cleared Devices
Recent clearances: THE ART OF INTIMACY RESPONSE PERSONAL LUBRICANT
1
Total
1
Cleared
0
Denied
Goodmark USA, Inc. has 1 FDA 510(k) cleared medical devices. Based in Southborough, US.
Historical record: 1 cleared submissions from 2005 to 2005. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Goodmark USA, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Goodmark USA, Inc.
1 devices