Neuroone Medical Technologies Corp. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Neuroone Medical Technologies Corp. has 4 FDA 510(k) cleared medical devices. Based in Eden Prairie, US.
Latest FDA clearance: Aug 2025. Active since 2021. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Neuroone Medical Technologies Corp. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Ostendorf Consulting, LLC and Mcra, LLC.
4 devices