ENDLESSFIBER REUSABLE SURGICAL LASER FIBER

ENDLESSFIBER REUSABLE SURGICAL LASER FIBER is an FDA 510(k)-cleared medical device (K140366) manufactured by Hogue Surgical, 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 August 14, 2014. Regulation: 8.