Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003909093

FEI Number

3003909093

Entity Name

BIOVIEW LTD.

City/State/Country

REHOVOT Central, IL

Establishment Address

3 PAKRIS STREET, REHOVOT Central 76702, IL

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

BIOVIEW LTD. (Owner Number: 9054795)

Owner / Operator Contact Address

3 Pekeris Street, --, Rehovot, IL-NOTA 7670203, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

BIOBLUE DROP BIOWHITE-SUPPLEMENT BIOWHITE BIOWHITE-AMNIO BIOBLUE BIOBLUE AMNIO

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
PPM	General Purpose Reagent	Pathology	Class 1	864.4010	2003-05-05

Official Correspondent

YUVAL HARARI

US Agent Details

David Kutas Business: BIOVIEW USA INC. Email: david@BIOVIEW.CO.IL Phone: (978) 6704741

Related Public Records

Same Entity

BIOVIEW 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 3003909093. Last updated year: 2026. Please use registration number 3003909093 when referencing this establishment in official correspondence.