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Home›Canada›AMICO DIAGNOSTIC INCORPORATED

AMICO DIAGNOSTIC INCORPORATED

Canada · Richmond Hill
✓ Record-verifiedregistrations found in 3 markets

This company has registrations in United States, Saudi Arabia, Canada — 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
5listed device types
Class I 2Class II 3Class III 0
plus 6 registration records and 1 510(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
2 including historic records
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 States6 registration records, 1 510(k), 0 PMA, 7 excluded
Saudi Arabia2 confirmed, 2 excluded
Canada0 confirmed, 2 excluded
Manufacturer names merged into this page: AMICO DIAGNOSTIC INCORPORATED · Amico Diagnostic Incorporated

Company information

Country
Canada
City
Richmond Hill

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

12014 · K131939

FDA listed device types

Ophthalmoscope, Ac-Powered 1Continuous Measurement Thermometer 1Blood Pressure Cuff 1Otoscope 1Stethoscope, Manual 1

Registration details (sample)

MarketIdentifierNameClass / date
USK131939AMICO DH-W35 OPHTHALMOSCOPE SERIES2014-03-26
SAME0000012450SFDAA00010STETHOSCOPES—
SAME0000012450SFDAA00011DIAGNOSTIC STATION—

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