Craniofacial Technologies, Inc. - FDA 510(k) Cleared Devices

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.