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Posted on 1/14/2021

B-TEMIA ASIA

B-Temia Inc. (the “Company”) announces that it received 510(k) clearance from the United States Food and Drug Administration for its powered human mobility device Keeogo™ Dermoskeleton System. This clearance opens the largest medical device market in the world.

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B-TEMIA INC. OBTAINS 510(K) CLEARANCE FOR KEEOGO™ FROM THE USA FOOD & DRUG ADMINISTRATION (FDA

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