Omniguide Beampath Laser Beam Delivery System

K062423 is the FDA 510(k) clearance record for OMNIGUIDE BEAMPATH LASER BEAM DELIVERY SYSTEM, a class II device, cleared for Omniguide, Inc. on 2006-09-21 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 22 510(k) clearances for Omni-Guide Holdings, Inc., from 2006-07-19 to 2023-04-21. As of 2026-09-10, FDA records show no recalls naming K062423.