
Laser Peripherals, LLC
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Laser Peripherals, LLC Family of Bare Laser Fibers is an FDA 510(k)-cleared medical device (K170366) manufactured by Laser Peripherals, 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 June 7, 2017. Regulation: 8.