REMY Medical Therapy Laser System

REMY Medical Therapy Laser System is an FDA 510(k)-cleared medical device (K190034) manufactured by Footdocprenur, 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 14, 2019. Regulation: 8.