Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008467514

FEI Number

3008467514

Entity Name

MODULARITE

City/State/Country

POLIGNY Bourgogne-Franche-Comte, FR

Establishment Address

3 AVENUE DE LA REPUBLIQUE, POLIGNY Bourgogne-Franche-Comte 39800, FR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

MODULARITE (Owner Number: 10044485)

Owner / Operator Contact Address

3 AVENUE DE LA REPUBLIQUE, POLIGNY, FR-BFC 39800, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Zenka Face&Cie

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2013-06-19

Official Correspondent

Ghislain BEUZON

US Agent Details

Sarah V Vinson Email: sales@lunetteusa.com Phone: (716) 5101209

Related Public Records

Same Entity

MODULARITE

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 3008467514. Last updated year: 2026. Please use registration number 3008467514 when referencing this establishment in official correspondence.