HomeKorea, RepublicMaxstar Industrial Co., Ltd.

Maxstar Industrial Co., Ltd.

Korea, Republic · Gimpo Gyeonggi
✓ Record-verifiedregistrations found in 3 markets

This company has registrations in United States, Brazil, Taiwan — 3 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
2listed device types
Class I 1Class II 1Class III 0
plus 6 registration records and 3 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
1registered devices
Class II 1
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
2valid device licences
Class II 2
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
pendingnot queried
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 States6 registration records, 3 510(k), 0 PMA
Brazil1 confirmed, 0 excluded
Manufacturer names merged into this page: MAXSTAR INDUSTRIAL CO LTD · MAXSTAR INDUSTRIAL CO. LTD

Company information

Country
Korea, Republic
City
Gimpo 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

12014 · K130385
12019 · K173158
12021 · K191441

FDA listed device types

Massager, Powered Inflatable Tube 1Massager, Therapeutic, Electric 1

Registration details (sample)

MarketIdentifierNameClass / date
USK191441Air Relax, Compressible Limb Sleeve System (Model: AR-1.0, AR-2.0)2021-03-05
USK173158Air Relax2019-05-30
USK130385COMPRESSIBLE LIMB SLEEVE SYSTEM2014-02-18
BR81955769001AIR RELAX PLUS MODELO AR-3.0Class II

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