Avation Medical, Inc., the innovator in patient-friendly, closed-loop neuromodulation options to treat life-altering medical conditions, announced that its Vivally System received US Food and Drug Administration (FDA) 510(k) clearance. Vivally is a non-invasive, bladder control therapy device and mobile application to treat patients with the conditions of urinary urgency and urge urinary incontinence (UUI) caused by overactive bladder (OAB) syndrome, without the need for surgery, drugs, or needle-electrodes. The Vivally System is the only closed-loop, non-invasive neuromodulation system for bladder control cleared for sale in the United States. Closed-loop control objectively confirms activation of the tibial nerve and continuously adjusts therapy parameters to ensure optimal output throughout the session.
“Millions of people suffer from urinary urgency and urge urinary incontinence who do not want invasive surgery or the unwanted side-effects of drugs,” said Jill Schiaparelli, Avation CEO. “With 30 minute at-home therapy sessions as little as once per week, and a mobile application with an electronic bladder diary and progress tracking, Vivally provides an effective treatment option that patients can easily fit into their schedule.”
Revolutionary smart bladder control system provides new option, allowing patients to conduct therapy at-home without surgery, implants, or drugs
Urinary urgency and UUI are the primary symptoms of OAB, a highly prevalent and debilitating chronic condition that is estimated to impact more than 42 million women and men in the United States. Despite the availability of several effective treatments, very low rates of patient adoption and poor therapy compliance persist.
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The Vivally System works by providing an electrical signal to the patient’s tibial nerve through an ankle-worn garment. A clinician creates a personalized therapy range for each patient and prescribes the Vivally System for use in the home. The Vivally Controller uses a proprietary closed-loop control algorithm and electromyography (EMG) to offer personalized therapy for each patient.
Vivally’s safety and effectiveness were evaluated in a prospective, multi-center clinical study of 96 subjects with overactive bladder (the FREEOAB Study). At 6 months, 69% of subjects were responders for urinary urgency and 63% for urge incontinence, where a responder is a subject showing at least 50% symptom improvement or a return to normal. 98% of subjects found the Vivally System easy to use. There were no significant device-related adverse events during the study.
