Sl3

K102639 is the FDA 510(k) clearance record for SL3, a class II device, cleared for Discus Dental, LLC on 2010-12-01 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 15 510(k) clearances for Discus Dental, LLC, from 2002-08-20 to 2010-12-01. As of 2026-09-10, FDA records show one recall naming K102639.