Lasemar 800, 1000, 1500

K092860 is the FDA 510(k) clearance record for LASEMAR 800, 1000, 1500, a class II device, cleared for Eufoton S.R.L. on 2010-07-16 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 2 510(k) clearances for Eufoton S.R.L., from 2010-07-16 to 2026-05-29. As of 2026-09-10, FDA records show no recalls naming K092860.