HomeChinaFoshan Gaunying Electronics Co., Ltd.

Foshan Gaunying Electronics Co., Ltd.

China · Foshan Guangdong
✓ Record-verifiedregistrations found in 5 markets

This company has registrations in United States, Australia, Hong Kong, Israel, 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 2Class II 2Class III 0
plus 8 registration records and 6 510(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
IIa 1
HKHong KongMDACS
2valid listings
Class II 2
ILIsraelAMAR
4registrations
RURussiaRoszdravnadzor
1active registrations
Class 2a 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 States8 registration records, 6 510(k), 0 PMA
Manufacturer names merged into this page: FOSHAN GAUNYING ELECTRONICS CO., LTD

Company information

Country
China
City
Foshan 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

12010 · K102149
22011 · K110721
12012 · K121154
22014 · K140211

FDA listed device types

Lamp, Infrared, Therapeutic Heating 1Nebulizer (Direct Patient Interface) 1Humidifier, Non-Direct Patient Interface (Home-Use) 1Nebulizer, Medicinal, Non-Ventilatory (Atomizer) 1

Registration details (sample)

MarketIdentifierNameClass / date
USK140211ULTRASONIC MESH NEBULIZER2014-05-30
USK132247ULTRASONIC MESH NEBULIZER2014-01-08
USK121154ULTRASONIC NEBULIZER2012-08-20

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