Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3030626336

FEI Number

3030626336

Entity Name

MAGENTIQ EYE LTD

City/State/Country

Haifa, IL

Establishment Address

6 Ben-Gurion Blvd., Haifa 3541416, IL

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

Magentiq Eye Ltd (Owner Number: 10090333)

Owner / Operator Contact Address

6 Ben-Gurion Blvd., Haifa, IL-HA 3541416, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K223473

PMA Number

N/A

All Registered Proprietary Names

ME-APDS MAGENTIQ-COLO

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
QNP	Gastrointesinal Lesion Software Detection System	Gastroenterology, Urology	Class 2	876.1520	2024-03-13

Official Correspondent

Dror Zur

US Agent Details

Robert J Duffy Business: Medical Device Post-Production Services, Inc. Email: bob.duffy@mdpps-inc.com Phone: (858) 4871859

Related Public Records

Same Entity

Magentiq Eye Ltd

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 3030626336. Last updated year: 2026. Please use registration number 3030626336 when referencing this establishment in official correspondence.