Beijing Winkonlaser Technology Limited is one of 2114 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Beijing Winkonlaser Technology Limited - FDA 510(k) Cleared Devices
Recent clearances: High Intensity Focused Electromagnetic Stimulation Device (FE60), Diode Laser Hair Removal System
2
Total
2
Cleared
0
Denied
Beijing Winkonlaser Technology Limited has 2 FDA 510(k) cleared medical devices. Based in Beijing, CN.
Latest FDA clearance: Aug 2026. Active since 2024. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Beijing Winkonlaser Technology Limited Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Beijing Believe-Med Technology Service Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Beijing Winkonlaser Technology Limited
2 devices