Vydence Family of Lasers

K252753 is the FDA 510(k) clearance record for Vydence Family of Lasers, a class II device, cleared for Vydence Medical Industria E Commercio Ltda on 2026-01-24 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 Vydence Medical Industria E Commercio Ltda. As of 2026-09-10, FDA records show no recalls naming K252753.