HomeIsraelCMT MEDICAL TECHNOLOGIES, LTD.

CMT MEDICAL TECHNOLOGIES, LTD.

Israel · Yoqne'Am Ilit
✓ Record-verifiedregistrations found in 4 markets

This company has registrations in United States, Canada, Taiwan, Israel — 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
3listed device types
Class I 0Class II 3Class III 0
plus 4 registration records and 12 510(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 6
7 including historic records
TWTaiwanTFDA
1valid device licences
Class II 1
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
2registrations
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, 12 510(k), 0 PMA, 2 excluded
Canada6 confirmed, 0 excluded
Manufacturer names merged into this page: CMT MEDICAL TECHNOLOGIES, LTD. · CMT MEDICAL TECHNOLOGIES LTD

Company information

Country
Israel
City
Yoqne'Am Ilit

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

11995
21996
11999
12000
12001
12008
12010
22011
12016
12020

FDA listed device types

System, X-Ray, Stationary 1Solid State X-Ray Imager (Flat Panel/Digital Imager) 1System, X-Ray, Fluoroscopic, Image-Intensified 1

Registration details (sample)

MarketIdentifierNameClass / date
USK202235ArtPIX DRF2020-09-03
USK162224ArtPix Mobile EZ2GO2016-09-22
USK110849PRESTODR 41432011-04-26
CA9559ADR 1000A/RF SYSTEMClass II
CA62129ADR 2000AClass II
CA63162ADR 1000A/E2 SYSTEMClass II

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