HomeKorea, RepublicLIBERTECH CORPORATION

LIBERTECH CORPORATION

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

This company has registrations in United States, Brazil, Saudi Arabia, Taiwan, Australia, Russia — 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
5listed device types
Class I 5Class II 0Class III 0
plus 5 registration records and 0 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
2registered devices
Class I 2
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
7registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
TWTaiwanTFDA
2valid device licences
Class I 2
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
1active ARTG entries
Class I 1
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
pendingnot queried
RURussiaRoszdravnadzor
1active registrations
Class 2a 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 States5 registration records, 0 510(k), 0 PMA
Brazil2 confirmed, 0 excluded
Saudi Arabia7 confirmed, 0 excluded
Manufacturer names merged into this page: LIBERTECH CORPORATION · Libertech Corporation

Company information

Country
Korea, Republic
City
Hwaseong-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 listed device types

Cushion, Flotation 1Orthosis, Limb Brace 1Protector, Skin Pressure 1Mattress, Flotation Therapy, Non-Powered 1Cushion, Wheelchair 1

Registration details (sample)

MarketIdentifierNameClass / date
BR80118040015ALMOFADA TERAPÊUTICA COMFORT CARE ORTOBRASClass I
BR80118040016ALMOFADA TERAPÊUTICA COMFORT CARE ORTOBRASClass I
SAME0000012587SFDAA00001Operating Room Gel Pads
SAME0000015600SFDAA00001Wheelchair Air Cushion

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