LaserDock, HolmiumDock, CO2Dock,OmniDock, KTPDock

LaserDock, HolmiumDock, CO2Dock,OmniDock, KTPDock is an FDA 510(k)-cleared medical device (K170215) manufactured by Patient Pocket, 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 18, 2017. Regulation: 8.