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Rewalk Robotics Ltd. Dba Lifeward

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
1
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K241822ReWalk® 7 Personal Exoskeleton (50-20-0005)March 12, 2025