HomeCanadaThornhill Research, Inc.

Thornhill Research, Inc.

Canada · Toronto
✓ Record-verifiedregistrations found in 6 markets

This company has registrations in United States, Canada, Singapore, Australia, Hong Kong, Israel — 6 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
6listed device types
Class I 0Class II 6Class III 0
plus 4 registration records and 5 510(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
0active device licences
4 including historic records
TWTaiwanTFDA
0valid device licences
SGSingaporeHSA SMDR
1device registrations
CLASS C 1
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
2active ARTG entries
IIb 2
HKHong KongMDACS
1valid listings
Class III 1
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 States4 registration records, 5 510(k), 0 PMA
Manufacturer names merged into this page: THORNHILL RESEARCH 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

12010 · K093261
12014 · K140049
12015 · K140264
12017 · K161420
12019 · DEN170044

FDA listed device types

Isocapnic Ventilation Device 1Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) 1Gas-Machine, Anesthesia 1Generator, Oxygen, Portable 1Ventilator, Emergency, Powered (Resuscitator) 1Pump, Portable, Aspiration (Manual Or Powered) 1

Registration details (sample)

MarketIdentifierNameClass / date
USDEN170044ClearMate2019-03-14
USK161420MOVES SLC2017-06-06
USK140264MADM2015-01-05

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