HomeCanadaWALSH MEDICAL DEVICES, INC.

WALSH MEDICAL DEVICES, INC.

Canada · Oakville
✓ 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
5listed device types
Class I 3Class II 2Class III 0
plus 4 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
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
1active device licences
Class III 1
4 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
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, 1 510(k), 0 PMA, 1 excluded
Canada1 confirmed, 0 excluded
Manufacturer names merged into this page: WALSH MEDICAL DEVICES, INC. · WALSH MEDICAL DEVICES INC.

Company information

Country
Canada
City
Oakville

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

12003 · K030158

FDA listed device types

Dilator, Lachrymal 1Crutch, Ptosis 1Transilluminator, Battery-Powered 1Electrosurgical, Cutting & Coagulation & Accessories 1Apparatus, Cautery, Radiofrequency, Ac-Powered 1

Registration details (sample)

MarketIdentifierNameClass / date
USK030158UNIT, CAUTERY, TEHRMAL,BATTERY-POWERED2003-07-17
CA6875PDT BALLON INFLATORClass III

Similar companies

3DBioFibR Inc.
Canada · markets 0
Actuonix Motion Devices Inc.
Canada · markets 0
ARTRON LABORATORIES INC
Canada · markets 8
Averna Powered by Spherea
Canada · markets 0
Batrik Medical Manufacturing, Inc.
Canada · markets 9
bioLytical Laboratories Inc.
Canada · markets 6
Is this your company? Claim the page, add information or report a data error.Claim / report an error →