ADMT is re-engineering it’s patented, non-invasive medical device used for the treatment and control of tinnitus, called the Aurex-3®, which was previously FDA-cleared. The new version of the device will be enhanced to state-of-the-art digital control, allowing for smartphone, tablet and cloud integration, expected to significantly improve patient usability and compliance. Additionally, the new Aurex-3® will include the ability to wirelessly monitor and forward patient progress directly to their physician. Once the redesign is completed the new version of the Aurex-3 will be submitted to the FDA for clearance.