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See today's BioWorld MedTech
Home » B-Temia gains traction with 510(k) clearance for mobility device
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B-Temia gains traction with 510(k) clearance for mobility device

Sep. 14, 2020
By Annette Boyle
B-Temia Inc.’s Keeogo mobility device is on the move in the U.S. now that it has received 510(k) clearance from the U.S. FDA. Unlike currently available exoskeletons that move for patients, the Keeogo (keep on going) Dermoskeleton system amplifies signals from patients who can initiate movement but need additional assistance.
BioWorld MedTech Regulatory Artificial intelligence Exoskeleton 510(k) FDA

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