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

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

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 ...

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

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

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

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 ...

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

The Florida Cancer Specialists & Research Institute (FCS) has introduced a liquid biopsy test to identify circulating cells ...

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