Craniofacial Technologies, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Craniofacial Technologies, Inc. has 1 FDA 510(k) cleared medical devices. Based in Bell Canyon, US.
Last cleared in 2022. Active since 2022. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Craniofacial Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Craniofacial Technologies, Inc.
1 devices