Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010598390

FEI Number

3010598390

Entity Name

FINLAY London

City/State/Country

London London, City of, GB

Establishment Address

61 Broadwick St, Soho, London London, City of W1F 9QT, GB

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Finlay and Company (Owner Number: 10045370)

Owner / Operator Contact Address

61 Broadwick St, London, GB-LND W1F 9QT, GB

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Finlay

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2016-12-21

Official Correspondent

David Lochead

US Agent Details

Ali Miller Email: a.rmiller@yahoo.com Phone: (319) 3339169

Related Public Records

Same Entity

Finlay and Company

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 3010598390. Last updated year: 2026. Please use registration number 3010598390 when referencing this establishment in official correspondence.