Craniofacial Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Craniofacial Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Ortholock Anchorage 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.
510(k) submissions have been managed by Nilo Medical Consulting Group as regulatory consultant.
FDA 510(k) Regulatory Record - Craniofacial Technologies, Inc.
1 devices