Lasermatic Supercombo(tm) Surgical Laser System

K903131 is the FDA 510(k) clearance record for LASERMATIC SUPERCOMBO(TM) SURGICAL LASER SYSTEM, a class II device, cleared for Lasermatic, Inc. on 1991-02-19 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 10 510(k) clearances for Lasermatic, Inc., from 1988-01-22 to 1991-02-19. As of 2026-09-10, FDA records show no recalls naming K903131.