The Society of Thoracic Surgeons (STS) in the US has introduced a mobile application, the STS Risk Calculator App.

New regulations from the UK’s MHRA around post-market surveillance (PMS) requirements for medical devices have come into ...

Italy-based Bracco Imaging and Subtle Medical have obtained an EU CE mark for AiMIFY, a jointly developed software designed ...

InspireMD’s CGuard Prime Embolic Prevention System (EPS) has secured CE Mark approval under the European MDR for stroke ...

Qiagen, Incyte have announced a master collaboration agreement to create a diagnostic panel to aid in the treatment of ...

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 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 ...

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

Mainz Biomed has started the feasibility phase of the PancAlert project to develop a pancreatic cancer screening test.

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