Dentos, Inc. - FDA 510(k) Cleared Devices
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.
FDA 510(k) cleared devices by Dentos, Inc.
2 devices