The US Food and Drug Administration (FDA) has granted 510(k) clearance to Viz.ai for its Viz Subdural Plus module.

This breakthrough shows that a robot’s outer skin can be reshaped, reused and remain functional - critical in human-robot ...

Epiminder has reported the outcomes from the landmark UMPIRE (sUb-scalp Monitoring ePileptic selzuREs) trial evaluating ...

Presidio Medical has received an IDE approval from the FDA, enabling a pivotal study of its neuromodulation platform.

Medtronic has announced a voluntary recall of select Newport HT70 and Newport HT70 Plus ventilators and certain related service parts.