Laser Peripherals, LLC Family of Bare Laser Fibers

K170366 is the FDA 510(k) clearance record for Laser Peripherals, LLC Family of Bare Laser Fibers, a class II device, cleared for Laser Peripherals, LLC on 2017-06-08 under FDA product code GEX (Powered Laser Surgical Instrument). FDA's definition for product code GEX reads: "A laser (light amplification by stimulated emission of radiation) based device having coherence, collimated and typically monochromatic radiation. Typically indicated to to cut, destroy, remove or coagulate tissue, generally soft tissue...". FDA records list 12 510(k) clearances for Laser Peripherals, LLC, from 1988-03-23 to 2017-06-08. As of 2026-09-10, FDA records show no recalls naming K170366.