HomeKorea, RepublicMICRO-NX CO., LTD.

MICRO-NX CO., LTD.

Korea, Republic · Dong-Gu Daegu
✓ Record-verifiedregistrations found in 5 markets

This company has registrations in United States, Taiwan, Australia, Israel, Russia — 5 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
4listed device types
Class I 4Class II 0Class III 0
plus 7 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
3valid device licences
Class I 3
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
4active ARTG entries
IIa 4
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
3registrations
RURussiaRoszdravnadzor
2active registrations
Class 2a 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 States7 registration records, 7 510(k), 0 PMA
Manufacturer names merged into this page: MICRO-NX CO., LTD.

Company information

Country
Korea, Republic
City
Dong-Gu Daegu

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

12017 · K161500
12020 · K192809
12021 · K201192
22022 · K220577
12023 · K232810
12025 · K231562

FDA listed device types

Handpiece, Direct Drive, Ac-Powered 1Handpiece, Belt And/Or Gear Driven, Dental 1Controller, Foot, Handpiece And Cord 1Handpiece, Contra- And Right-Angle Attachment, Dental 1

Registration details (sample)

MarketIdentifierNameClass / date
USK231562ELEC ENGINE (Model: ISE-170L)2025-07-18
USK232810Dental Handpiece, Wireless Endodontic Handpiece, endoit2023-11-09
USK220577Dental Handpiece, Model CA160, CA160L, and CA500L2022-07-29

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