LED Light Therapy Device, ELIXIR MD™

K241293 is the FDA 510(k) clearance record for LED Light Therapy Device, ELIXIR MD™, a class II device, cleared for Yassen Wellness, LLC on 2024-07-08 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 Yassen Wellness, LLC. As of 2026-09-10, FDA records show no recalls naming K241293.