FDAnews
www.fdanews.com/articles/193424-sky-medicals-geco-device-cleared-for-marketing
ClearanceStamp_Blue.gif

Sky Medical’s Geco Device Cleared for Marketing

November 12, 2019

UK-based Sky Medical Technology received 510(k) clearance from the FDA for its geko device for stimulation of the calf muscles to prevent venous thrombosis in non-surgical patients at risk for venous thromboembolism (VTE).

The device was previously cleared for immediate post-surgical stimulation of calf muscles to prevent VTE, increasing blood circulation and edema reduction.

The geko is a battery powered, wearable device the size of a wristwatch and worn at the knee. It stimulates the common peroneal nerve activating the calf and foot muscle pumps, resulting in increased blood flow in the deep veins of the calf.

View today's stories