Model Md-25 CO2 Laser for Podiatry Applications

K881587 is the FDA 510(k) clearance record for MODEL MD-25 CO2 LASER FOR PODIATRY APPLICATIONS, a class II device, cleared for Laser Engineering, Inc. on 1988-06-03 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 18 510(k) clearances for Laser Engineering, Inc., from 1988-06-03 to 2022-09-22. As of 2026-09-10, FDA records show no recalls naming K881587.