HomeChinaA & I INDUSTRIES LTD

A & I INDUSTRIES LTD

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

This company has registrations in United States, Brazil, Taiwan, Australia, Israel — 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
35listed device types
Class I 35Class II 0Class III 0
plus 36 registration records and 4 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
1registered devices
Class I 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
1valid device licences
Class I 1
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
6active ARTG entries
Class I 6
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 States36 registration records, 4 510(k), 0 PMA, 731 excluded
Brazil1 confirmed, 103 excluded
Saudi Arabia0 confirmed, 78 excluded
Canada0 confirmed, 65 excluded
Manufacturer names merged into this page: A & I INDUSTRIES LTD · A&I INDUSTRIES LTD.

Company information

Country
China
City
Foshan City 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

11995 · K941066
21997 · K954577
12004 · K041652

FDA listed device types

showing 8 of 35
Chair, Surgical, Non-Electrical 1Stretcher, Hand-Carried 1Armrest, Wheelchair 1Regulator, Pressure, Gas Cylinder 1Device, Anti-Tip, Wheelchair 1Lift, Patient, Non-Ac-Powered 1Chair, Geriatric 1Cane, Safety Walk 1

Registration details (sample)

MarketIdentifierNameClass / date
USK041652ACUPUNCTURE NEEDLES2004-12-29
USK954577WS FREQUENCY SPECTRUM EFFECT PHYSIATRICS APPARATUS1997-05-09
USK970574ACUPUNCTURE NEEDLES1997-04-24
BR80026710006CADEIRA DE BANHO PARA PORTADORES DE DEFICIÊNCIA FÍSICAClass I

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