
Fiberlase U.S.A.
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FIBERLAS 100 MEDICAL SYSTEM is an FDA 510(k)-cleared medical device (K833499) manufactured by Fiberlase U.S.A.. 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 1, 1984. Regulation: 8.