Rewalk Robotics Ltd. Dba Lifeward

Rewalk Robotics Ltd. Dba Lifeward holds 1 FDA 510(k) medical device clearance, cleared in 2025.

Top product codes for Rewalk Robotics Ltd. Dba Lifeward

PHL — Physical Medicine1 device

Recent clearances by Rewalk Robotics Ltd. Dba Lifeward

K241822 — ReWalk® 7 Personal Exoskeleton (50-20-0005)Code PHL·2025-03-12

Data sourced from openFDA. This site is unofficial and independent of the FDA.