Model Mm-2405 and Mm-2410 Copper Vapor Laser

K921298 is the FDA 510(k) clearance record for MODEL MM-2405 AND MM-2410 COPPER VAPOR LASER, a class II device, cleared for Cj Laser Corp. on 1992-07-02 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 Cj Laser Corp. As of 2026-09-10, FDA records show no recalls naming K921298.