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Zynex Obtains FDA 510(k) Clearance For InWave Medical Device - Quick Facts

8/30/2012 9:21 AM ET

Zynex Inc. (ZYXI.OB), a provider and developer of non-invasive medical devices for electrotherapy, stroke rehabilitation, neurological diagnosis and cardiac monitoring, announced that it received FDA 510(k) clearance on its InWave medical device. This device is used primarily for treating female urinary incontinence. Incontinence is defined as the involuntary loss of bladder or bowel control.

According to the National Association for Continence, urinary incontinence affects 200 million people world-wide, and it is believed that 80% of those sufferers are women.

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by RTT Staff Writer

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