HomeKorea, RepublicCHIYEWON CO., LTD.

CHIYEWON CO., LTD.

Korea, Republic · Guri-Si Gyeonggi
✓ Record-verifiedregistrations found in 6 markets

This company has registrations in United States, Taiwan, Singapore, 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
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 1 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
1valid device licences
Class III 1
SGSingaporeHSA SMDR
1device registrations
CLASS D 1
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
2active ARTG entries
Class III 2
HKHong KongMDACS
1valid listings
Class IV 1
ILIsraelAMAR
4registrations
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 States1 registration records, 1 510(k), 0 PMA
Manufacturer names merged into this page: CHIYEWON CO., LTD.

Company information

Country
Korea, Republic
City
Guri-Si Gyeonggi

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

12015 · K140021

FDA listed device types

Bone Grafting Material, Animal Source 1

Registration details (sample)

MarketIdentifierNameClass / date
USK140021TI-OSS2015-06-05

Similar companies

A-ZoneTech Co., LTD
Korea, Republic · markets 0
AB Medical, Inc.
Korea, Republic · markets 8
Ace Medical Co., Ltd
Korea, Republic · markets 9
AIT Studio Co., Ltd.
Korea, Republic · markets 1
AITRICS CO.,LTD
Korea, Republic · markets 2
Allmedicus Co., Ltd.
Korea, Republic · markets 4
Is this your company? Claim the page, add information or report a data error.Claim / report an error →