Dentamerica is one of 20659 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dentamerica - FDA 510(k) Cleared Devices
Recent clearances: ENDOMAX CORDLESS ENDODONTIC HANDPIECE, DIGIREX DIGITAL DENTAL RADIOGRAPHY SYSTEM, SCALEX 800
4
Total
4
Cleared
0
Denied
Dentamerica has 4 FDA 510(k) cleared medical devices. Based in Industry, US.
Historical record: 4 cleared submissions from 1996 to 2010. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Dentamerica Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dentamerica
4 devices