CO2 Laser Machine, Model: BW-203B

K211735 is the FDA 510(k) clearance record for CO2 Laser Machine, Model: BW-203B, a class II device, cleared for Zhengzhou Bestview ST Co., Ltd. on 2021-10-22 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 Zhengzhou Bestview ST Co., Ltd., from 2021-07-28 to 2021-10-22. As of 2026-09-10, FDA records show no recalls naming K211735.