LIFEWARD, INC.

FDA Device Registration & Listing · Marlborough, MA, US · Registration 3009767053

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
3009767053
FEI Number
3009767053
Entity Name
LIFEWARD, INC.
City/State/Country
Marlborough, MA, US
Establishment Address
200 DONALD LYNCH BLVD, Marlborough, MA 01752, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198
Owner / Operator
Lifeward, Inc. (Owner Number: 10043289)
Owner / Operator Contact Address
200 Donald Lynch Boulevard, Marlborough, MA 01752, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K200032
PMA Number
N/A

All Registered Proprietary Names

Rewalk ReWalk-I

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PHL Powered Exoskeleton Physical Medicine Class 2 890.3480 2014-12-20
BXB Exerciser, Powered Physical Medicine Class 1 890.5380 2013-02-03
PHL Powered Exoskeleton Physical Medicine Class 2 890.3480 2020-10-06

Official Correspondent

Miri Pariente

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Lifeward, Inc.
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 3009767053. Last updated year: 2026. Please use registration number 3009767053 when referencing this establishment in official correspondence.
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