Dentos, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dentos, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Absoanchor Microimplant
2
Total
2
Cleared
0
Denied
Dentos, Inc. has 2 FDA 510(k) cleared medical devices. Based in Ann Arbor, US.
Historical record: 2 cleared submissions from 2006 to 2019. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Dentos, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Onbix Corporation as regulatory consultant.
FDA 510(k) Regulatory Record - Dentos, Inc.
2 devices