Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3044546258

FEI Number

3044546258

Entity Name

VIZO SPECS LTD

City/State/Country

Petakh Tikva Central, IL

Establishment Address

24, Hasivim, Petakh Tikva Central 4959382, IL

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

VIZO SPECS LTD (Owner Number: 10095368)

Owner / Operator Contact Address

HaSivim 24, Petah Tikva, IL-M 4959382, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

VZARI-Frame

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2026-03-18

Official Correspondent

Yael Richter

US Agent Details

Alan Minsk Business: Arnall Golden Gregory LLP Email: alan.minsk@agg.com Phone: (404) 8738690

Related Public Records

Same Entity

VIZO SPECS LTD

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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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3044546258. Last updated year: 2026. Please use registration number 3044546258 when referencing this establishment in official correspondence.