Solon

K221766 is the FDA 510(k) clearance record for Solon, a class II device, cleared for Lmg Lasers Comercio, Importacao E Exportacao Ltda on 2024-01-05 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 Lmg Lasers Comercio, Importacao E Exportacao Ltda. As of 2026-09-10, FDA records show no recalls naming K221766.