SkinStylus SteriLock MicroSystem

SkinStylus SteriLock MicroSystem is an FDA 510(k)-cleared medical device (K200044) manufactured by Esthetic Education, 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 April 9, 2020. Regulation: 8.