HomeCanadaSpectral Medical, Inc.

Spectral Medical, Inc.

Canada · Toronto
✓ Record-verifiedregistrations found in 4 markets

This company has registrations in United States, Canada, Taiwan, Russia — 4 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
2listed device types
Class I 1Class II 1Class III 0
plus 2 registration records and 2 510(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
1active device licences
Class II 1
3 including historic records
TWTaiwanTFDA
1valid device licences
Class I 1
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
pendingnot queried
RURussiaRoszdravnadzor
1active registrations
Class 1 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 States2 registration records, 2 510(k), 0 PMA, 7 excluded
Brazil0 confirmed, 1 excluded
Canada1 confirmed, 1 excluded
Manufacturer names merged into this page: Spectral Medical Inc. · SPECTRAL MEDICAL INC.

Company information

Country
Canada
City
Toronto

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

12017 · K170790
12019 · K183176

FDA listed device types

Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use 1Assay, Endotoxin Activity, Chemiluminescent 1

Registration details (sample)

MarketIdentifierNameClass / date
USK183176Endotoxin Activity Assay (EAA)2019-03-12
USK170790SAM CRRT Unit, SAM Cassette CRRT2017-12-13
CA61083TOX STATUS SCREEN TESTClass II

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