Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015168845

FEI Number

3015168845

Entity Name

Lifewand. LTD.

City/State/Country

Ein-Vered Central, IL

Establishment Address

CTG Building Ha Yarden St, Ein-Vered Central 4069600, IL

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Lifewand Ltd (Owner Number: 10059390)

Owner / Operator Contact Address

CTG Building Ha Yarden St, Ein-Vered, IL-NOTA 4069600, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

LIFEWAND

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GCX	Apparatus, Suction, Operating-Room, Wall Vacuum Powered	General Hospital	Class 2	880.6740	2019-01-01

Official Correspondent

Yaron Leifenberg

US Agent Details

George Hattub Business: Medicsense USA, LLC. Email: ghattub@comcast.net Phone: (508) 4796116

Related Public Records

Same Entity

Lifewand 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 3015168845. Last updated year: 2026. Please use registration number 3015168845 when referencing this establishment in official correspondence.