Erchonia Evrl Laser

K050672 is the FDA 510(k) clearance record for ERCHONIA EVRL LASER, a class II device, cleared for Erchonia Medical, Inc. on 2005-05-02 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 11 510(k) clearances for Erchonia Medical, Inc., from 2004-09-30 to 2016-06-03. As of 2026-09-10, FDA records show no recalls naming K050672.