Neuroone Medical Technologies Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neuroone Medical Technologies Corp. - FDA 510(k) Cleared Devices
Recent clearances: OneRF Trigeminal Nerve Radiofrequency Probes, OneRF Ablation System, Evo® sEEG System
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.
FDA 510(k) Regulatory Record - Neuroone Medical Technologies Corp.
4 devices