The device, called the Geko, is a wristwatch sized product that stimulates the peroneal nerve through electrical signals that lead to muscle activation of the lower limb, where DVT commonly occurs. The device is self-adhesive and is applied to the back of the knee without wires or leads. Although not FDA approved and not for sale in the U.S., Geko is CE Marked in Europe under the Medical Devices Directive.
Related Articles on Medical Devices:
FDA, CDC and AAO to Monitor Cataract Surgery Devices to Stop TASS Outbreaks
Medical Device Industry Spent Almost $32M Lobbying Congress in Third Quarter
NASA to Use da Vinci Surgical Robotics to Fix Satellites
At the Becker’s 32nd Annual Meeting: The Business and Operations of ASCs, taking place October 29-31 in Chicago, ASC leaders, surgeons and healthcare executives will explore strategies to drive growth, enhance operational performance, navigate reimbursement challenges and prepare for the future of ambulatory surgery. Apply for complimentary registration now.