HomeChinaShenzhen Gsd Tech Co., Ltd.

Shenzhen Gsd Tech Co., Ltd.

China · Shenzhen Guangdong
✓ Record-verifiedregistrations found in 4 markets

This company has registrations in United States, Brazil, Australia, Israel — 4 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
5listed device types
Class I 1Class II 4Class III 0
plus 8 registration records and 7 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
1registered devices
Class II 1
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
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
2active ARTG entries
IIa 1IIb 1
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
1registrations
RURussiaRoszdravnadzor
pendingnot queried
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 States8 registration records, 7 510(k), 0 PMA, 1 excluded
Brazil1 confirmed, 0 excluded
Manufacturer names merged into this page: SHENZHEN GSD TECH CO., LTD

Company information

Country
China
City
Shenzhen Guangdong

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

12009
12015
12018
12019
12020
12021
12023

FDA listed device types

Light, Microscope 1Powered Light Based Non-Laser Surgical Instrument With Thermal Effect 1Light, Ultraviolet, Dermatological 1Powered Laser Surgical Instrument 1Light Based Over-The-Counter Hair Removal 1

Registration details (sample)

MarketIdentifierNameClass / date
USK230060Light Based Hair Removal Device GP5922023-03-03
USK213225Diode Laser System GP900A8, Diode Laser System GP900Q82021-12-22
USK202827308nm Excimer UV-light Skin Therapy System2020-12-15
BR80726749011SPOTS PARA RADIOFREQUÊNCIAClass II

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