PicoLazer Laser System

PicoLazer Laser System is an FDA 510(k)-cleared medical device (K192583) manufactured by Rohrer Aesthetics, 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 January 16, 2020. Regulation: 8.