Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

8043830

FEI Number

3009220474

Entity Name

FRANCIS KLEIN SAS

City/State/Country

PARIS, FR

Establishment Address

35 Boulevard Henri IV, PARIS 75004, FR

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

FRANCIS KLEIN SAS (Owner Number: 9004074)

Owner / Operator Contact Address

35 Boulevard Henri IV, PARIS, FR-75 75004, FR

Initial Importer Flag

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
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2000-02-22

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

FRANCIS KLEIN 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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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 8043830. Last updated year: 2026. Please use registration number 8043830 when referencing this establishment in official correspondence.