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

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.