Rewalk Robotics Ltd. Dba Lifeward
1 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| ReWalk® 7 Personal Exoskeleton (50-20-0005) (K241822) | Rewalk Robotics Ltd. Dba Lifeward | 2025-03-12 |
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Every clearance here is in the API, with alerts when new ones post.