Ortholock Anchorage Devices

Ortholock Anchorage Devices is an FDA 510(k)-cleared medical device (K202691) manufactured by Craniofacial Technologies, Inc.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 27, 2022. Regulation: 8.