JIMMY FAIRLY

FDA Device Registration & Listing · Paris, FR · Registration 3014518341

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
3014518341
FEI Number
3014518341
Entity Name
JIMMY FAIRLY
City/State/Country
Paris, FR
Establishment Address
23 Rue Du Mail, Paris F-75002, FR
Establishment Type(s)
Remanufacture Medical Device,Develop Specifications But Do Not Manufacture At This Facility,Repack or Relabel Medical Device,Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Jimmy Fairly (Owner Number: 10090335)
Owner / Operator Contact Address
23 Rue Du Mail, Paris, FR-75 F-75002, FR
Initial Importer Flag
N
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 2024-03-13
NJH Lens, Spectacle (Prescription), For Reading Discomfort Ophthalmic Class 1 886.5844 2024-03-13
HQG Lens, Spectacle, Non-Custom (Prescription) Ophthalmic Class 1 886.5844 2024-03-13

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

Jimmy Fairly
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 3014518341. Last updated year: 2026. Please use registration number 3014518341 when referencing this establishment in official correspondence.
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