DeepX DermoSight Dermatoscope

DeepX DermoSight Dermatoscope is an FDA 510(k)-cleared medical device (K230448) manufactured by Deepx Health, LLC. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 16, 2023. Regulation: 8.