Sky Medical Technology wins new FDA license to market new W3 geko ™ device for venous insufficiency and ischemia

This latest (W3) geko ™ device 510 (k) is licensed under the Company’s 2021 FDA’s W2 geko ™ device as well as for venous insufficiency and / or ischemia. The new (W3) geko ™ device clearance brings 3 more benefitsrd Electrode, increased patient access (nerve stimulation), patient comfort and better patient outcomes – and to … Read more