Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014285231

FEI Number

3014285231

Entity Name

BIOPROTECT LTD.

City/State/Country

Netanya Central, IL

Establishment Address

Ha Gavish 6, Netanya Central 4250706, IL

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Bioprotect Ltd. (Owner Number: 10088617)

Owner / Operator Contact Address

Ha Gavish 6, Netanya, IL-M 4250706, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K222972

PMA Number

N/A

All Registered Proprietary Names

Bioprotect Balloon Implant

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OVB	Hydrogel Spacer	Radiology	Class 2	892.5725	2023-08-31

Official Correspondent

George Hattub

US Agent Details

George Hattub Business: Medicsense USA LLC Email: ghattub@outlook.com Phone: (508) 4796116

Related Public Records

Same Entity

Bioprotect 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 3014285231. Last updated year: 2026. Please use registration number 3014285231 when referencing this establishment in official correspondence.