Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3002420106

FEI Number

3002420106

Entity Name

Manufacture Kering Eyewear

City/State/Country

SUCY EN BRIE Val-de-Marne, FR

Establishment Address

1, rue Benjamin FRANKLIN, SUCY EN BRIE Val-de-Marne 94370, FR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Manufacture Kering Eyewear (Owner Number: 10023250)

Owner / Operator Contact Address

1, rue Benjamin Franklin, Sucy-en-brie, FR-94 94370, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

CARTIER

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2007-11-13

Official Correspondent

DHONDT Remy

US Agent Details

Francesco Merlo Email: francesco.merlo@kering.com Phone: (201) 5876566

Related Public Records

Same Entity

Manufacture Kering Eyewear

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 3002420106. Last updated year: 2026. Please use registration number 3002420106 when referencing this establishment in official correspondence.