Grafenberg Labs is one of 5063 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Grafenberg Labs - FDA 510(k) Cleared Devices
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.
FDA 510(k) Regulatory Record - Grafenberg Labs
1 devices