Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007632745

FEI Number

3007632745

Entity Name

BEST DESIGNERS, INC.

City/State/Country

Doral, FL, US

Establishment Address

1500 NW 89th Ct Ste 216, Doral, FL 33172, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

BEST DESIGNERS, INC. (Owner Number: 10029677)

Owner / Operator Contact Address

1500 NW 89TH CT # 216, Miami, FL 33172, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Best Designer Inc Best Designer Inc

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2014-02-21
HOI	Spectacle, Magnifying	Ophthalmic	Class 1	886.5840	2015-03-03

Official Correspondent

Richard Knowles

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

BEST DESIGNERS, 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
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007632745. Last updated year: 2026. Please use registration number 3007632745 when referencing this establishment in official correspondence.