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Bioness Inc. Receives FDA Clearance of Its NESS L300 Plus System
Date:5/10/2011

tient's course of therapy and allow home users better control over their knee and foot, making it easier to walk. Bioness continues to be committed to bringing innovative solutions to patients and in setting the standard of care with our advanced technology. The NESS L300 Plus represents yet another product in our pursuit of this mission."

Bioness will display the NESS L300 Plus at the upcoming Annual Conference & Exposition of the American Physical Therapy Association (APTA) June 9th – 11th at National Harbor, Maryland in Booth #419. The Company anticipates the device will become commercially available to neurorehabilitation hospitals and centers around the country and to consumers for home use within the coming weeks.

About Bioness Inc.

Bioness provides neuromodulation technologies that help improve lives and restore function for those living with neurological deficits and peripheral pain. The Company develops, manufactures and markets innovative neuromodulation products that help individuals with central nervous system disorders such as stroke, multiple sclerosis, spinal cord injury and traumatic brain injury regain movement in affected limbs. The NESS L300® Foot Drop System and NESS H200® Hand Rehabilitation System, and NESS L300® Plus System are cleared for use by the Food and Drug Administration and are designed to help patients achieve new levels of physical independence and productivity. Individual results vary. Consult with a qualified physician to find out if these products are right for you. Additional information about Bioness can be found at www.bioness.com.

NESS®, NESS L300®, NESS L300® Plus, Bioness® are trademarks of Bioness Inc. | www.bioness.com | Rx Only

Media Contact:

Wendy Ryan/Genevieve Gadenne
Schwartz Communications
781-684-0770

SOURCE Bioness Inc.
Copyright©2010 PR Newswire.
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