HomeKorea, RepublicShinhung MST Co., Ltd.

Shinhung MST Co., Ltd.

Korea, Republic · Wonju Si Gangwon
✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Russia — 2 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
8listed device types
Class I 6Class II 2Class III 0
plus 13 registration records and 7 510(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
0valid device licences
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
pendingnot queried
RURussiaRoszdravnadzor
1active registrations
Class 2b 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 States13 registration records, 7 510(k), 0 PMA, 1 excluded
Manufacturer names merged into this page: Shinhung MST Co., Ltd.

Company information

Country
Korea, Republic
City
Wonju Si Gangwon

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

12013 · K123155
12016 · K160106
12017 · K162867
12020 · K200189
32023 · K221752

FDA listed device types

Attachment, Precision, All 1Tray, Impression, Preformed 1Accessories, Implant, Dental, Endosseous 1Handle, Instrument, Dental 1Elevator, Surgical, Dental 1Drill, Dental, Intraoral 1Implant, Endosseous, Root-Form 1Abutment, Implant, Dental, Endosseous 1

Registration details (sample)

MarketIdentifierNameClass / date
USK221752Stella2023-06-04
USK223395Luna Dental Implant System2023-02-03
USK221317S-Mono2023-01-13

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