HomeChinaNINGBO VERYKIND MEDICAL DEVICE CO., LTD.

NINGBO VERYKIND MEDICAL DEVICE CO., LTD.

China · Ningbo Zhejiang
✓ Record-verifiedregistrations found in 6 markets

This company has registrations in United States, Brazil, South Korea, 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
pendingnot queried
EUEuropean UnionEUDAMED
pendingnot queried
USUnited StatesFDA openFDA
2listed device types
Class I 0Class II 2Class III 0
plus 2 registration records and 2 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
10registered devices
Class II 10
17 including historic records
SASaudi ArabiaSFDA
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
1GMP quality-system certificates
Import 1
AUAustraliaTGA ARTG
4active ARTG entries
IIa 2IIb 2
HKHong KongMDACS
2valid listings
Class II 1Class III 1
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 States2 registration records, 2 510(k), 0 PMA
Brazil10 confirmed, 0 excluded
Manufacturer names merged into this page: NINGBO VERYKIND MEDICAL DEVICE CO., LTD. · NINGBO VERYKIND MEDICAL DEVICE CO., LTD

Company information

Country
China
City
Ningbo Zhejiang

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

22021 · K211458

FDA listed device types

Staple, Implantable 1Stapler, Surgical 1

Registration details (sample)

MarketIdentifierNameClass / date
USK211458Disposable Anorectal Staplers, Disposable Intraluminal Staplers, Disposable Linear Cutting Staplers, Disposable Endoscopic Cutting Staplers2021-12-30
USK202709Disposable Powered Endoscopic Linear Cutting Staplers and Cartridges2021-05-18
BR81787039001Trocarte Descartável PCDClass II
BR81787039002Trocarte Descartável PDQ PDQLClass II
BR81787039003Trocarte Descartável DavidClass II

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