Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3043513144

FEI Number

3043513144

Entity Name

CARDINE DESIGNS, LLC

City/State/Country

Santa Clarita, CA, US

Establishment Address

21864 Parvin Dr, Santa Clarita, CA 91350, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Cardine Designs (Owner Number: 10095120)

Owner / Operator Contact Address

24844 Ave. Rockefeller, Valencia, CA 91355, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Cardine Designs Optical Frames

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2026-01-26

Official Correspondent

javan diaz

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Cardine Designs

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 3043513144. Last updated year: 2026. Please use registration number 3043513144 when referencing this establishment in official correspondence.