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BioWorld - Tuesday, March 17, 2026
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Home » Ekso steps up with FDA clearance for exoskeleton use in MS
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Ekso steps up with FDA clearance for exoskeleton use in MS

June 14, 2022
By Annette Boyle
Ekso Bionics Holdings Inc. added a new indication for its robotic Eksonr exoskeleton with a U.S. FDA 510(k) clearance for use of the mobility device in patients with multiple sclerosis (MS). The green light for MS follows clearances for stroke and spinal cord rehabilitation in 2016 and acquired brain injury (ABI) in 2020.
Medical technology Regulatory Exoskeleton Neurology/psychiatric U.S. 510(k) FDA

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