Dermascan Laser Surgical Handpiece

K860083 is the FDA 510(k) clearance record for DERMASCAN LASER SURGICAL HANDPIECE, a class II device, cleared for Medical Laser Research & Development Corp. on 1986-08-07 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 one 510(k) clearance for Medical Laser Research & Development Corp. As of 2026-09-10, FDA records show no recalls naming K860083.