Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3004145084

FEI Number

3004145084

Entity Name

OPTIK K & R INC.

City/State/Country

Toronto Ontario, CA

Establishment Address

425 Midwest Road, Toronto Ontario M1P3A6, CA

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

OPTIK K & R Inc. (Owner Number: 10045451)

Owner / Operator Contact Address

425 Midwest Road, Toronto, CA-ON M1P3A6, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K943753

PMA Number

N/A

All Registered Proprietary Names

Ophthalmic Spectacle Frame

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2021-06-01

Official Correspondent

Ryan Maxwell

US Agent Details

Bret Andre Business: EYEREG CONSULTING INC. Email: bandre@fdapproval.com Phone: (503) 3725226

Related Public Records

Same Entity

OPTIK K & R 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 3004145084. Last updated year: 2026. Please use registration number 3004145084 when referencing this establishment in official correspondence.