FDA Device Establishments · JSON-LD · Markdown

Lifeward LTD.

FEI 3007615665 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active

FEI Number3007615665
Owner / OperatorLifeward LTD. (#10033624)
Address3 Hatnufa St. (6th Floor), Upper Yokneam Northern, 00206-9203, IL
Mandatory US AgentLIFEWARD, INC.
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)PHL
Regulation § (21 CFR)890.3480
Proprietary namesReWalk® 7 Personal Exoskeleton (50-20-0005)

External sources

Source: openFDA. Public-domain (CC0).