Optica 60 Nd;yag Surgical Laser System

K912703 is the FDA 510(k) clearance record for OPTICA 60 ND;YAG SURGICAL LASER SYSTEM, a class II device, cleared for Xintec Corporation on 1991-10-11 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 26 510(k) clearances for Xintec Corporation, from 1990-09-20 to 2010-02-03. As of 2026-09-10, FDA records show no recalls naming K912703.