HomeChinaHuachenyang (Shenzhen) Technology Co. , Ltd.

Huachenyang (Shenzhen) Technology Co. , Ltd.

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

This company has registrations in United States, Australia, Hong Kong, 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
7listed device types
Class I 7Class II 0Class III 0
plus 7 registration records and 1 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
0registered devices
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
1active ARTG entries
IVD Class 1 1
HKHong KongMDACS
1valid listings
IVD C 1
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 States7 registration records, 1 510(k), 0 PMA
Manufacturer names merged into this page: HUACHENYANG(SHENZHEN)TECHNOLOGY 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

12022 · K212856

FDA listed device types

Container, Specimen Mailer And Storage, Sterile 1Container, Specimen, Sterile 1Culture Media, Non-Propagating Transport 1Container, Specimen Mailer And Storage, Non-Sterile 1General Purpose Reagent 1Applicator, Absorbent Tipped, Sterile 1Culture Media, Non-Selective And Non-Differential 1

Registration details (sample)

MarketIdentifierNameClass / date
USK212856iClean Viral Transport System (VTM-RT kit)2022-08-18

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