Beijing Syntech Laser Co., Ltd. is one of 2150 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Beijing Syntech Laser Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: DIODE LASER, APOLLO V+ MEDICAL PLATFORM, APOLLO IV+ MEDICAL PLATFORM, NICE STATION LIGHT BASED PLATFORM, TRIXEL CO2 LASER
3
Total
3
Cleared
0
Denied
Beijing Syntech Laser Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Shanghai, CN.
Historical record: 3 cleared submissions from 2011 to 2013. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Beijing Syntech Laser Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Beijing Syntech Laser Co., Ltd.
3 devices