Lafont

FDA Device Registration & Listing · Paris Ile-de-France, FR · Registration 9680773

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
9680773
FEI Number
3003149673
Entity Name
Lafont
City/State/Country
Paris Ile-de-France, FR
Establishment Address
33 Bvd Du General Martial Valin, Paris Ile-de-France 75015, FR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Lafont (Owner Number: 9011307)
Owner / Operator Contact Address
33 Bvd Du General Martial Valin, --, Paris, FR-IDF 75015, FR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Sun

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HQZ Frame, Spectacle Ophthalmic Class 1 886.5842 1994-08-29

Official Correspondent

No official correspondent registered.

US Agent Details

Desiree Jewsbury Business: Lafont Co Email: djewsbury@lafontusa.com Phone: (212) 6249966

Related Public Records

Same Entity

Lafont
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 9680773. Last updated year: 2026. Please use registration number 9680773 when referencing this establishment in official correspondence.
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