HomeUSAC.A.I. Industries Corp.

C.A.I. Industries Corp.

USA · Alhambra
✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Brazil — 2 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable
CNChinaNMPA
n/aThis registry lists domestic registrants only
EUEuropean UnionEUDAMED
pendingnot queried
USUnited StatesFDA openFDA
41listed device types
Class I 38Class II 3Class III 0
plus 42 registration records and 5 510(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
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
pendingnot queried
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 States42 registration records, 5 510(k), 0 PMA, 729 excluded
Brazil1 confirmed, 103 excluded
Saudi Arabia0 confirmed, 78 excluded
Canada0 confirmed, 65 excluded
Manufacturer names merged into this page: A & I INDUSTRIES LTD · C & J INDUSTRIES, INC. · A&I INDUSTRIES LTD.

Company information

Country
USA
City
Alhambra

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

11988 · K880485
11995 · K941066
21997 · K954577
12004 · K041652

FDA listed device types

showing 8 of 41
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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