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RegeneCure Starts Clinical Study Using Polymeric Bone Stimulating Membrane for Dental Implants
Date:6/18/2013

ed a 510(k) application to the FDA in April 2012 for an initial trauma indication. The privately owned company has manufacturing facility meeting the high production standards required by European and United States authorities. In 2012, the company received ISO 13485:2003 certification.

For more information visit  http://www.regenecure.co.il or contact: Dr. Harry Langbeheim, VP Business Development, harry@regenecure.co.il, Tel: +972-2-5401013


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