MG DEVELOPPEMENT

FDA Device Registration & Listing · mauguio Herault, FR · Registration 3006979687

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
3006979687
FEI Number
3006979687
Entity Name
MG DEVELOPPEMENT
City/State/Country
mauguio Herault, FR
Establishment Address
178 rue negue cat, ZA Aeroport, mauguio Herault 34130, FR
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
MG Developpement (Owner Number: 10025161)
Owner / Operator Contact Address
178 rue negue cat, mauguio, FR-34 34130, FR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JRJ Unit, Drying Clinical Chemistry Class 1 862.2050 2008-11-20
EPN Pump, Nebulizer, Manual Ear, Nose, Throat Class 1 874.5220 2008-03-19
ESD Hearing Aid, Air-Conduction, Prescription Ear, Nose, Throat Class 1 874.3300 2013-04-25
EFX Protector, Silicate Dental Class 1 872.6670 2008-11-20
LRJ Disinfectant, Medical Devices General Hospital Class 1 880.6890 2008-03-19

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

MG Developpement
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
K892457 Telstar Electronics, Inc. TELSTAR MODEL 1/3 ITE HEARING AID 1989-06-06
K760996 Unitron Industries, Inc. HEARING AID (MODEL 695D, 905 & 960P) 1976-11-16
K840825 Maico Hearing Instruments, Inc. SERIES MR IN-THE-EAR CUSTOM HEARING AID 1984-03-30
K946253 Maico Hearing Instruments, Inc. MAICO IN-THE-EAR MODEL RD 201 1995-01-30
K863975 Gn Danavox, Inc. CUSTOM IN-THE-EAR 1986-11-07

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006979687. Last updated year: 2026. Please use registration number 3006979687 when referencing this establishment in official correspondence.
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