Optilite IX Laser Surgery Accessories

K992866 is the FDA 510(k) clearance record for OPTILITE IX LASER SURGERY ACCESSORIES, a class II device, cleared for Convergent Laser Technologies on 1999-11-18 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 2 510(k) clearances for Convergent Laser Technologies, from 1999-11-18 to 2021-11-09. As of 2026-09-10, FDA records show 2 recalls naming K992866.