HomeJapanNEMOTO KYORINDO CO., LTD.

NEMOTO KYORINDO CO., LTD.

Japan · Bunkyo-Ku
✓ Record-verifiedregistrations found in 9 markets

This company has registrations in United States, Canada, Taiwan, Singapore, South Korea, Australia, Hong Kong, Israel, Russia — 9 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
1listed device types
Class I 0Class II 1Class III 0
plus 3 registration records and 8 510(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
4 including historic records
TWTaiwanTFDA
3valid device licences
Class II 3
SGSingaporeHSA SMDR
5device registrations
CLASS C 5
KRSouth KoreaMFDS GMP
1GMP quality-system certificates
Import 1
AUAustraliaTGA ARTG
6active ARTG entries
Class I 1IIb 5
HKHong KongMDACS
3valid listings
Class III 3
ILIsraelAMAR
3registrations
RURussiaRoszdravnadzor
2active registrations
Class 2b 2
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 States3 registration records, 8 510(k), 0 PMA
Canada1 confirmed, 0 excluded
Manufacturer names merged into this page: NEMOTO KYORINDO CO., LTD.

Company information

Country
Japan
City
Bunkyo-Ku

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

12005
12006
12007
22010
12014
12018
12024

FDA listed device types

Injector And Syringe, Angiographic 1

Registration details (sample)

MarketIdentifierNameClass / date
USK242212Disposable Syringe (Kit); Nemoto Disposable Syringe (Kit)2024-08-27
USK173450PRESS DUO elite, PRESS DUO elite AG2018-02-07
USK133189DUAL SHOT ALPHA 72014-06-30
CA79001DUAL SHOT ALPHAClass II

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