WEIL INDUSTRIES

FDA Device Registration & Listing · Duttlenheim Bas-Rhin, FR · Registration 3030130442

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
3030130442
FEI Number
3030130442
Entity Name
WEIL INDUSTRIES
City/State/Country
Duttlenheim Bas-Rhin, FR
Establishment Address
83 rue de la gare, Zone Industrielle, Duttlenheim Bas-Rhin 67120, FR
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Weil Industries (Owner Number: 10091540)
Owner / Operator Contact Address
83 rue de la gare, Zone Industrielle, Duttlenheim, FR-67 67120, FR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Axilum Robotics 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 2024-10-14

Official Correspondent

Stephane Gerard

US Agent Details

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

Related Public Records

Same Entity

Weil Industries
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 3030130442. Last updated year: 2026. Please use registration number 3030130442 when referencing this establishment in official correspondence.
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