Grafenberg Labs is one of 19031 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Grafenberg Labs - FDA 510(k) Cleared Devices
Recent clearances: O Glide Personal Lubricant
1
Total
1
Cleared
0
Denied
Grafenberg Labs has 1 FDA 510(k) cleared medical devices. Based in New York, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Grafenberg Labs Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mjrac as regulatory consultant.
FDA 510(k) Regulatory Record - Grafenberg Labs
1 devices