Auxo A300, A150 and APod

Auxo A300, A150 and APod is an FDA 510(k)-cleared medical device (K220543) manufactured by Auxo Hair, LLC. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 19, 2022. Regulation: 8.