# Lifeward LTD.

FEI: 3007615665
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: Lifeward LTD. (#10033624)

Address: 3 Hatnufa St. (6th Floor), Upper Yokneam Northern, 00206-9203, IL

Mandatory US Agent: LIFEWARD, INC.

## Products

Total registered: 1
Top product codes: PHL
Regulation §: 890.3480

Proprietary names: ReWalk® 7 Personal Exoskeleton (50-20-0005)

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223007615665%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3007615665