Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3035364025

FEI Number

3035364025

Entity Name

FFF IMPORT INC

City/State/Country

New York, NY, US

Establishment Address

980 Madison Ave, New York, NY 10075, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198

Owner / Operator

FFF IMPORT INC (Owner Number: 10092491)

Owner / Operator Contact Address

980 Madsion Ave, New York, NY 10075, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ME+EM

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2025-01-24

Official Correspondent

Shannon Whitt

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

FFF IMPORT INC

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
3013507321	DEM FACTORY S.R.L.	Limana Belluno, IT
3015243992	L.G.R SRL	Roma, IT

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3035364025. Last updated year: 2026. Please use registration number 3035364025 when referencing this establishment in official correspondence.