HomeGermanyMAG & MORE GMBH

MAG & MORE GMBH

Germany · Munich Bavaria
✓ Record-verifiedregistrations found in 5 markets

This company has registrations in United States, Taiwan, Australia, Hong Kong, Israel — 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
2listed device types
Class I 0Class II 2Class III 0
plus 3 registration records and 5 510(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
1valid device licences
Class II 1
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
1active ARTG entries
IIa 1
HKHong KongMDACS
2valid listings
Class II 2
ILIsraelAMAR
1registrations
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 States3 registration records, 5 510(k), 0 PMA, 1 excluded
Brazil0 confirmed, 2 excluded
Canada0 confirmed, 1 excluded
Manufacturer names merged into this page: MAG & MORE GMBH

Company information

Country
Germany
City
Munich Bavaria

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

12018 · K180313
12024 · K232639
22025 · K243700
12026 · K260560

FDA listed device types

Transcranial Magnetic Stimulator 1Transcranial Magnetic Stimulation System For Obsessive-Compulsive Disorder 1

Registration details (sample)

MarketIdentifierNameClass / date
USK260560Apollo TMS Therapy System;Apollo light TMS Therapy System2026-05-22
USK243700Apollo TMS Therapy System2025-09-04
USK243539Apollo TMS Therapy System2025-08-18

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