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

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 ...

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

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

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

The US Food and Drug Administration (FDA) has granted 510(k) clearance to TYBR Health’s bioresorbable B3 GEL System.

Amid ongoing trade policy debates, leaders from the medtech industry convened on Capitol Hill alongside the Advanced Medical ...

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

A Northwestern Medicine-developed AI radiology tool has been shown to enhance productivity and swiftly detect ...

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

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