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.

Spanish company Aortyx has secured €13.8m ($15.8m) in a Series A financing round to further develop its bioresorbable patch, ...

GE HealthCare has released software combining its own imaging functionalities with tools enabled by a platform developed by ...

The US FDA has granted 510(k) clearance to Neurent Medical's NEUROMARK System for the treatment of individuals with chronic ...

Wandercraft has raised $75m in a Series D funding round to introduce the self-balancing personal exoskeleton, Eve, to market ...

Cognito has reported outcomes from a post hoc analysis of its OVERTURE trial, indicating that the Spectris AD can slow the ...

Somnee announced that it has secured $10m in a seed extension round to advance its AI-powered neurotech sleep wearables.

The health secretary addressed NHS employees a day after the £29bn NHS funding was announced. A £29bn investment into the ...