Dual Yellow Laser, Model D10b

K023899 is the FDA 510(k) clearance record for DUAL YELLOW LASER, MODEL D10B, a class II device, cleared for Norseld Pty., Ltd. on 2003-02-20 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 Norseld Pty., Ltd., from 2003-02-20 to 2004-05-27. As of 2026-09-10, FDA records show no recalls naming K023899.