Lifeward LTD.

FDA Device Registration & Listing · Upper Yokneam Northern, IL · Registration 3007615665

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3007615665
FEI Number
3007615665
Entity Name
Lifeward LTD.
City/State/Country
Upper Yokneam Northern, IL
Establishment Address
3 Hatnufa St. (6th Floor), Upper Yokneam Northern 00206-9203, IL
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Lifeward LTD. (Owner Number: 10033624)
Owner / Operator Contact Address
Hatnufa 3, Yokneaam, IL-Z 2069203, IL
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

ReWalk(TM) Personal ReWalk® 7 Personal Exoskeleton (50-20-0005) Rewalk(TM) Rehabilitation

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PHL Powered Exoskeleton Physical Medicine Class 2 890.3480 2016-08-04
PHL Powered Exoskeleton Physical Medicine Class 2 890.3480 2020-10-06
PHL Powered Exoskeleton Physical Medicine Class 2 890.3480 2025-12-17
PHL Powered Exoskeleton Physical Medicine Class 2 890.3480 2014-08-03

Official Correspondent

Miri Pariente

US Agent Details

Mark Grant Business: LIFEWARD, INC. Email: mark.grant@golifeward.com Phone: (704) 9420936

Related Public Records

Same Entity

Lifeward 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 3007615665. Last updated year: 2026. Please use registration number 3007615665 when referencing this establishment in official correspondence.
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