Medical Device Manufacturer · US , Eden Prairie , MN

Neuroone Medical Technologies Corp. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2021
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.

FDA 510(k) cleared devices by Neuroone Medical Technologies Corp.

4 devices
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