Lq1106 Ophthalmic Yag Laser

K882772 is the FDA 510(k) clearance record for LQ1106 OPHTHALMIC YAG LASER, a class II device, cleared for Keeler Instruments, Inc. on 1988-08-26 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 60 510(k) clearances for Keeler Instruments, Inc., from 1981-06-23 to 2019-02-08. As of 2026-09-10, FDA records show no recalls naming K882772.