Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1000454074

FEI Number

1000454074

Entity Name

Morel France SAS

City/State/Country

MORBIER Jura, FR

Establishment Address

117 ROUTE DES BUCLETS, MORBIER Jura 39400, FR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Morel France SAS (Owner Number: 9092441)

Owner / Operator Contact Address

117 ROUTE DES BUCLETS, --, MORBIER, FR-NOTA 39400, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Frames

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	1997-10-16

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

Morel France SAS

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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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1000454074. Last updated year: 2026. Please use registration number 1000454074 when referencing this establishment in official correspondence.