Sol Portable Diode Laser Unit (with Wireless Foot Control)

K141838 is the FDA 510(k) clearance record for SOL PORTABLE DIODE LASER UNIT (WITH WIRELESS FOOT CONTROL), a class II device, cleared for Regulatory Technology Services, LLC on 2014-07-25 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 Regulatory Technology Services, LLC, from 2014-06-04 to 2014-07-25. As of 2026-09-10, FDA records show no recalls naming K141838.