Beijing Honkon Technologies Co., Ltd. is one of 2152 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Beijing Honkon Technologies Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Slimming Treatment Device, DIODE LASER FOR HIAR REMOVAL, CO2 FRACTIONAL LASER
5
Total
5
Cleared
0
Denied
Beijing Honkon Technologies Co., Ltd. has 5 FDA 510(k) cleared medical devices. Based in Guangzhou, Guangdong, CN.
Historical record: 5 cleared submissions from 2013 to 2017. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Beijing Honkon Technologies Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Beijing Believe Technology Service Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Beijing Honkon Technologies Co., Ltd.
5 devices
Cleared
Mar 02, 2017
Slimming Treatment Device
General & Plastic Surgery
234d
Cleared
Apr 24, 2014
DIODE LASER FOR HIAR REMOVAL
General & Plastic Surgery
308d
Cleared
Jan 22, 2014
CO2 FRACTIONAL LASER
General & Plastic Surgery
216d
Cleared
Jan 16, 2014
Q-SWITCHED ND:YAG LASER
General & Plastic Surgery
206d
Cleared
Oct 18, 2013
MULTIFUNCTIONAL SERIES
General & Plastic Surgery
116d