Diamond Nd:yag Ophthalmic Laser

K901636 is the FDA 510(k) clearance record for DIAMOND ND:YAG OPHTHALMIC LASER, a class II device, cleared for Biovision, Inc. on 1990-06-22 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 6 510(k) clearances for Biovision, Inc., from 1990-06-22 to 2004-11-16. As of 2026-09-10, FDA records show no recalls naming K901636.