FDA 510(k) Clearance Received!

We are very excited to announce that we have officially received the 510(k) clearance from the FDA for our Recovr Rehabilitation System! The clearance was received in record time, less than four months after we submitted our application. Many thanks go to our consultant Kathryn Becker for her significant assistance with this process. The clearance is a critical step for us in commercializing our technology since the FDA considers our system an unclassified medical device.