Promident, LLC is one of 18445 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Promident, LLC - FDA 510(k) Cleared Devices
Recent clearances: Clear Blue Digi LED Curing Light, CHALLENGER/CLASSIC PUSH BUTTON HANDPIECE
2
Total
2
Cleared
0
Denied
Promident, LLC has 2 FDA 510(k) cleared medical devices. Based in New City, US.
Historical record: 2 cleared submissions from 2008 to 2017. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Promident, LLC Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Intertek Testing Services and Third Party Review Group, LLC.
FDA 510(k) Regulatory Record - Promident, LLC
2 devices