HomeIsraelMedoc Corp.

Medoc Corp.

Israel · Ramat Yishai Northern
✓ Record-verifiedregistrations found in 7 markets

This company has registrations in United States, Taiwan, Singapore, South Korea, Hong Kong, Israel, Russia — 7 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 4Class II 1Class III 0
plus 5 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
0active device licences
TWTaiwanTFDA
2valid device licences
Class II 2
SGSingaporeHSA SMDR
1device registrations
CLASS B 1
KRSouth KoreaMFDS GMP
2GMP quality-system certificates
Business type not stated 1Import 1
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
2valid listings
Class II 2
ILIsraelAMAR
1registrations
RURussiaRoszdravnadzor
1active registrations
Class 2a 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 States5 registration records, 1 510(k), 0 PMA, 1 excluded
Canada0 confirmed, 1 excluded
Manufacturer names merged into this page: MEDOC LTD.

Company information

Country
Israel
City
Ramat Yishai Northern

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

11993 · K922052

FDA listed device types

Vibrator, Therapeutic 1Test, Temperature Discrimination 1Dynamometer, Nonpowered 1Device, Vibration Threshold Measurement 1Evoked Potential Stimulator, Thermal 1

Registration details (sample)

MarketIdentifierNameClass / date
USK922052TSA 2001 THERMAL SENSORY ANALYZER1993-10-21

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