HomeChinaAlltion (Guangxi) Instrument Co., Ltd.

Alltion (Guangxi) Instrument Co., Ltd.

China · Wuzhou City Guangxi
✓ Record-verifiedregistrations found in 6 markets

This company has registrations in United States, Saudi Arabia, Taiwan, Australia, Israel, Russia — 6 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
8listed device types
Class I 6Class II 2Class III 0
plus 8 registration records and 0 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
0registered devices
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
2registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
TWTaiwanTFDA
7valid device licences
Class I 7
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
1active ARTG entries
Class I 1
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
5registrations
RURussiaRoszdravnadzor
2active registrations
Class 1 1Class 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, 0 510(k), 0 PMA
Saudi Arabia2 confirmed, 0 excluded
Manufacturer names merged into this page: Alltion (Guangxi) Instrument Co., Ltd. · Alltion (Guangxi) Instrument Co., Ltd

Company information

Country
China
City
Wuzhou City Guangxi

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 listed device types

Loupe, Diagnostic/Surgical 1Microscope, Surgical 1Microscope, Operating & Accessories, Ac-Powered, Ophthalmic 1Headlamp, Operating, Battery-Operated 1Device, Medical Examination, Ac Powered 1Light, Microscope 1Colposcope (And Colpomicroscope), Exempt 1Colposcope (And Colpomicroscope) 1

Registration details (sample)

MarketIdentifierNameClass / date
SAME0000016351SFDAA00001Surgical Microscope
SAME0000017392SFDAA00003Surgical Microscope

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