Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014318504

FEI Number

3014318504

Entity Name

MATTHIEU DUCHENE DESIGN

City/State/Country

Bruxelles Brussels-Capital Region, BE

Establishment Address

154 Avenue Dailly, Bruxelles Brussels-Capital Region 1030, BE

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Repack or Relabel Medical Device,Manufacture Medical Device,Remanufacture Medical Device

Owner / Operator

Matthieu Duchene Design (Owner Number: 10062020)

Owner / Operator Contact Address

154 Avenue Dailly, Bruxelles, BE-BRU 1030, BE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Matttew

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2019-12-11

Official Correspondent

Matthieu Duchene

US Agent Details

Herve Foulard Email: hfoulard@gmail.com Phone: (917) 9291001

Related Public Records

Same Entity

Matthieu Duchene Design

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
K910951	United Optical, Spa	OPTHLAMIC FRAMES	1991-05-06

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3009554831	ROGER EYE DESIGN	Etten-Leur Noord-Brabant, NL
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014318504. Last updated year: 2026. Please use registration number 3014318504 when referencing this establishment in official correspondence.