HomeTaiwanEMG TECHNOLOGY CO., LTD.

EMG TECHNOLOGY CO., LTD.

Taiwan · Taichung
✓ Record-verifiedregistrations found in 4 markets

This company has registrations in United States, Canada, Australia, Israel — 4 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
6listed device types
Class I 1Class II 5Class III 0
plus 10 registration records and 11 510(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
7 including historic records
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
1active ARTG entries
IIa 1
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
5registrations
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 States10 registration records, 11 510(k), 0 PMA, 1 excluded
Brazil0 confirmed, 1 excluded
Canada1 confirmed, 0 excluded
Manufacturer names merged into this page: EMG TECHNOLOGY CO., LTD.

Company information

Country
Taiwan
City
Taichung

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

32003
12004 · K042349
22005 · K043520
32006 · K063448
12008 · K072634
12011 · K112421

FDA listed device types

Apparatus, Suction, Ward Use, Portable, Ac-Powered 1Nebulizer (Direct Patient Interface) 1Bottle, Collection, Vacuum 1Generator, Oxygen, Portable 1Compressor, Air, Portable 1Tourniquet, Nonpneumatic 1

Registration details (sample)

MarketIdentifierNameClass / date
USK112421EMG SUCTION UNIT2011-09-01
USK072634EMG TRITON -COMP,MODEL NCA01-XXX SERIES2008-11-19
USK063448EMG AC/DC SUCTION UNIT2006-11-30
CA90669POWER NEB IIClass II

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