Coltene AG is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Coltene AG - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Coltene AG has 2 FDA 510(k) cleared medical devices. Based in Mahwah, US.
Historical record: 2 cleared submissions from 2002 to 2004. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Coltene AG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Coltene AG
2 devices