Axilum Robotics

FDA Device Registration & Listing · Schiltigheim Grand Est, FR · Registration 3014805507

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3014805507
FEI Number
3014805507
Entity Name
Axilum Robotics
City/State/Country
Schiltigheim Grand Est, FR
Establishment Address
21 avenue de l'Europe, Schiltigheim Grand Est 67300, FR
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Axilum Robotics (Owner Number: 10060211)
Owner / Operator Contact Address
21 avenue de l'Europe, Schiltigheim, FR-GES 67300, FR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

TMS-Cobot TS MV

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QFF Electromechanical Arm For A Transcranial Magnetic Stimulation System Neurology Class 2 882.5805 2019-04-11

Official Correspondent

Michel Berg

US Agent Details

Stephan Toupin Business: Dawa Medical LLC Email: stoupin@dawamedical.com Phone: (305) 5999373

Related Public Records

Same Entity

Axilum Robotics
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014805507. Last updated year: 2026. Please use registration number 3014805507 when referencing this establishment in official correspondence.
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