HomeKorea, RepublicRemed Co., Ltd

Remed Co., Ltd

Korea, Republic · Cheongju-si · www.remed.kr
✓ Record-verifiedregistrations found in 10 marketsEU SRN KR-MF-000008128

This company has registrations in European Union, United States, United Kingdom, Canada, Taiwan, Singapore, Australia, Hong Kong, Israel, Russia — 10 overseas markets. EU UDI-DI records ≥1, the first 300 verified individually. 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
≥1UDI-DI device records
Class IIa 1
large result set — only the first 300 records were verified, so the real figure is at least this
USUnited StatesFDA openFDA
2listed device types
Class I 0Class II 2Class III 0
plus 5 registration records and 3 510(k)
UKUnited KingdomMHRA PARD
1registered device records
Class IIa 1
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
TWTaiwanTFDA
9valid device licences
Class II 8Class III 1
SGSingaporeHSA SMDR
1device registrations
CLASS B 1
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
3active ARTG entries
IIa 3
HKHong KongMDACS
1valid listings
Class III 1
ILIsraelAMAR
2registrations
RURussiaRoszdravnadzor
9active registrations
Class 2a 4Class 2b 5
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.

European Union1,146 raw hits, 299 excluded, 1 confirmed. Large result set — only the first 300 verified
United States5 registration records, 3 510(k), 0 PMA, 1 excluded
United Kingdom1 confirmed, 14 excluded
Brazil0 confirmed, 1 excluded
Canada1 confirmed, 2 excluded
Manufacturer names merged into this page: REMED Co., Ltd. · REMED CO., LTD.

Regulatory identity

EU manufacturer SRN
KR-MF-000008128
EU authorised representative
Obelis s.a.
UK responsible person
PHOENIX HEALTHCARE PRODUCTS LTD

Company information

Country
Korea, Republic
City
Cheongju-si
Website
www.remed.kr
Product categories
Clinical Diagnostics & Therapeutic TechnologiesOrthopaedics, Trauma & RehabilitationPhysiotherapy equipment

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.

Business registration

KRX ticker code
302550
Registration status
Active
Incorporated
2019-12-06

Business registration data from KRX KIND, retrieved 2026-09-02. Public registry information only; details of directors and shareholders are not collected.

FDA 510(k) clearances by year

22021 · K202537
12022 · K220625

FDA listed device types

Transcranial Magnetic Stimulator 1Stimulator, Muscle, Powered 1

Registration details (sample)

MarketIdentifierNameClass / date
EU08809308380720Smart TMTClass IIa
UK58762COMPACT IIClass IIa
USK220625ALTMS Magnetic Stimulation Therapy System, Blossom TMS Therapy System2022-04-06
USK202537ALTMS Magnetic Stimulation Therapy System2021-11-26
USK202031Talent-Pro Electromagnetic Stimulator2021-05-06
CA89099SALUS-TALENT ELECTRO-MAGNETIC STIMULATORClass II

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