HomeChinaBEIJING HONKON TECHNOLOGIES CO., LTD.

BEIJING HONKON TECHNOLOGIES CO., LTD.

China · Beijing
✓ Record-verifiedregistrations found in 5 markets

This company has registrations in United States, Brazil, Canada, Australia, Russia — 5 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable
CNChinaNMPA
pendingnot queried
EUEuropean UnionEUDAMED
pendingnot queried
USUnited StatesFDA openFDA
4listed device types
Class I 1Class II 3Class III 0
plus 5 registration records and 5 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
3registered devices
Class II 3
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
1 including historic records
TWTaiwanTFDA
0valid device licences
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
13active ARTG entries
IIa 2IIb 11
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
pendingnot queried
RURussiaRoszdravnadzor
1active registrations
Class 2b 1
Not yet connected: India CDSCO, Indonesia Kemenkes. The public search for Japan PMDA and Vietnam IMDA does not return manufacturer names, so entries cannot be linked to companies coming — where there is no data it is shown as "pending", never estimated.

How these numbers were verified

record-verified

Company-name search in every official database is a substring match and returns same-named but different companies. Each figure below is the count after re-checking every record against the manufacturer name.

United States5 registration records, 5 510(k), 0 PMA
Brazil3 confirmed, 0 excluded
Manufacturer names merged into this page: BEIJING HONKON TECHNOLOGIES CO., LTD. · BEIJING HONKON TECHNOLOGIES CO.,LTD

Company information

Country
China
City
Beijing

Fields marked "pending" have not been obtained yet; that does not mean they do not exist. Risk records (litigation, penalties, operating anomalies) are kept internal and not published.

FDA 510(k) clearances by year

12013 · K131859
32014 · K131838
12017 · K161892

FDA listed device types

Massager, Therapeutic, Electric 1Powered Light Based Non-Laser Surgical Instrument With Thermal Effect 1Powered Laser Surgical Instrument 1Massager, Vacuum, Light Induced Heating 1

Registration details (sample)

MarketIdentifierNameClass / date
USK161892Slimming Treatment Device2017-03-02
USK131838DIODE LASER FOR HIAR REMOVAL2014-04-24
USK131837CO2 FRACTIONAL LASER2014-01-22
BR80841510001EQUIPAMENTO PARA DEPILAÇÃOClass II
BR80963310001EQUIPAMENTO PARA DEPILAÇÃOClass II
BR80358300017EQUIPAMENTO PARA DEPILAÇÃO DPILClass II

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