Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012823347

FEI Number

3012823347

Entity Name

MAG & MORE GMBH

City/State/Country

Munich Bavaria, DE

Establishment Address

Machtlfinger Strasse 13, Munich Bavaria 81379, DE

Establishment Type(s)

Manufacture Medical Device,Complaint File Establishment per 21 CFR 820.198

Owner / Operator

MAG & More GmbH (Owner Number: 10057820)

Owner / Operator Contact Address

Machtlfinger Strasse 13, Munich, DE-BY 81379, DE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K260560

PMA Number

N/A

All Registered Proprietary Names

Apollo light TMS Therapy System Apollo TMS Pro Apollo TMS Therapy System

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OBP	Transcranial Magnetic Stimulator	Neurology	Class 2	882.5805	2026-05-26

Official Correspondent

Juliane Riess

US Agent Details

German American Chamber of Commerce, Inc. German American Ch Email: legalservices@gaccny.com Phone: (212) 9748830

Related Public Records

Same Entity

MAG & More GmbH

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K243700	Mag & More GmbH	Apollo TMS Therapy System	2025-09-04
K231926	Neuronetics, Inc.	NeuroStar Advanced Therapy System (All previously cleared models)	2024-03-22

Similar Registrations

Registration Number	Establishment Name	Location
3018708317	MAGNUS MEDICAL INC.	Burlingame, CA, US
3039167582	NEUROMODULATORY DEVICES & APPLICATIONS (NMDA), INC	San Diego, CA, US
3007147067	NEXSTIM PLC	Helsinki Uusimaa, FI
3003144120	SPARTRONICS STRONGSVILLE, INC.	Strongsville, OH, US
8021774	THE MAGSTIM COMPANY LTD.	Carmarthenshire Wales, GB

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012823347. Last updated year: 2026. Please use registration number 3012823347 when referencing this establishment in official correspondence.