Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3031081959

FEI Number

3031081959

Entity Name

RETINALOGIK INC.

City/State/Country

Calgary Alberta, CA

Establishment Address

3655 36 street NW, Calgary Alberta T2L 1Y8, CA

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

RetinaLogik Inc. (Owner Number: 10090291)

Owner / Operator Contact Address

3655 36 street NW, Calgary, CA-AB T2L 1Y8, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

RVF200 RVF200 RVF200

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HOX	Chart, Visual Acuity	Ophthalmic	Class 1	886.1150	2024-03-27
HIT	Tester, Color Vision	Ophthalmic	Class 1	886.1170	2024-03-27
QTO	Digital Visual Acuity Test	Ophthalmic	Class 1	886.1150	2026-04-02

Official Correspondent

Julia St.Amand

US Agent Details

Scott Bednar Business: QA/RA CONSULTING GROUP, INC. Email: sbednar@qaraconsultinggroup.com Phone: (412) 4188066

Related Public Records

Same Entity

RetinaLogik Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3031081959. Last updated year: 2026. Please use registration number 3031081959 when referencing this establishment in official correspondence.