Ekso™ (version 1.1) and Ekso GT™ (version 1.2)

Ekso™ (version 1.1) and Ekso GT™ (version 1.2) is an FDA 510(k)-cleared medical device (K161443) manufactured by Ekso Bionics, Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 18, 2016. Regulation: 8.