Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3021192255

FEI Number

3021192255

Entity Name

FIZE Medical LTD.

City/State/Country

Modiin Central, IL

Establishment Address

Hasdera Hamerkazit 15, Modiin Central 7173004, IL

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Fize Medical Ltd. (Owner Number: 10083656)

Owner / Operator Contact Address

Hasdera Hamerkazit 15, Modiin, IL-M 7173004, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

FIZE kUO

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EXY	Uroflowmeter	Gastroenterology, Urology	Class 2	876.1800	2021-12-09

Official Correspondent

Hani Rauch

US Agent Details

Ron Melts Business: MarketWinch Inc. Email: ron@marketwinch.com Phone: (833) 3073979

Related Public Records

Same Entity

Fize Medical 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 3021192255. Last updated year: 2026. Please use registration number 3021192255 when referencing this establishment in official correspondence.