VaporMAX LDD; MOJo LDD; MegaJOULE LDD

VaporMAX LDD; MOJo LDD; MegaJOULE LDD is an FDA 510(k)-cleared medical device (K233157) manufactured by Innovaquartz, 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 2, 2024. Regulation: 8.