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Rewalk Robotics Ltd. Dba Lifeward

FDA 510(k) & PMA Approved Devices — 1 products

Total Devices1
Categories1
Latest Approval2025-03-12
TypeNumberDevice NameCodeDate
510(k) K241822 ReWalk® 7 Personal Exoskeleton (50-20-0005) PHL 2025-03-12 View