Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3019567818

FEI Number

3019567818

Entity Name

KIMEZE ENTERPRISES LIMITED

City/State/Country

Newbury West Berkshire, GB

Establishment Address

2 Old Bath Road,, Newbury West Berkshire RG14 1QL, GB

Establishment Type(s)

Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Kimeze Enterprises Limited (Owner Number: 10081877)

Owner / Operator Contact Address

184 SHEPHERDS BUSH ROAD, LONDON, GB-NOTA W6 7NL, GB

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Sunglasses in metal and acetate Glasses Frames in metal and acetate

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HOY	Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)	Ophthalmic	Class 1	886.4750	2021-06-04
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2021-06-04

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

Kimeze Enterprises Limited

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 3019567818. Last updated year: 2026. Please use registration number 3019567818 when referencing this establishment in official correspondence.