HomeUSAALLIANCE MEDICAL PRODUCTS, INC.

ALLIANCE MEDICAL PRODUCTS, INC.

USA · Irvine
✓ Record-verifiedregistrations found in 3 markets

This company has registrations in United States, Canada, Taiwan — 3 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
1listed device types
Class I 0Class II 0Class III 0unclassified 1
plus 1 registration records and 47 510(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
6active device licences
Class II 5Class III 1
TWTaiwanTFDA
1valid device licences
Class III 1
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 States1 registration records, 47 510(k), 0 PMA, 33 excluded
Brazil0 confirmed, 5 excluded
Saudi Arabia0 confirmed, 1 excluded
Canada6 confirmed, 7 excluded
Manufacturer names merged into this page: ALLIANCE MEDICAL PRODUCTS, INC. · ALLIANCE MEDICAL INC

Company information

Country
USA
City
Irvine

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

11994
11996
11999
102001
52002
102003
12004
112005
62006
12007

FDA listed device types

Media, Corneal Storage 1

Registration details (sample)

MarketIdentifierNameClass / date
USK060648REPROCESSED PHACOEMULSIFICATION TIPS2007-03-19
USK061045REPROCESSED ELECTROPHYSIOLOGY CATHETERS2006-08-31
USK051438VANGUARD REPROCESSED COMPRESSION GARMENTS (HILL-ROM)2006-04-04
CA6894ECHO 1000Class II
CA7409AKHO 5000Class II
CA8271AMIB7Class II

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