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

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

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

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

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

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

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 ...

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

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