The UK’s Labour Government has revealed its ’10-Year Health Plan’ for the country’s National Health Service (NHS). Speaking at a community health centre in London, Health Secretary Wes Streeting ...

The US Food and Drug Administration (FDA) has granted 510(k) clearance for Philips’ SmartSpeed Precise deep learning reconstruction software.

Intuitive’s multiport robotic-assisted surgical system, da Vinci 5, has secured the CE mark approval for use in adult and paediatric patients.

Cognito Therapeutics has reached its enrolment goal for the HOPE Study investigating the Spectris AD system for Alzheimer's disease (AD).

The UK Government is pushing for a single, unified digital patient record within the NHS, but experts have shared cybersecurity concerns.

Kardium has raised C$340m ($250m) to support the launch of its Globe pulsed field (PF) System for treating atrial fibrillation (AFib).

Fasikl has received 510(k) clearance from the FDA for its Felix NeuroAI Wristband, designed to address tremor-related functional ...

Carthera has received an orphan medical device status endorsement for its SonoCloud ultrasound system for treating brain ...

InterShunt has initiated the EASE HF2 early feasibility study of the InterShunt percutaneous atrial shunt catheter (PAS-C) system.

Philips has announced the expansion of its collaboration with Medtronic, focusing on advancing patient monitoring ...

The US FDA has granted 510(k) clearance to PathAI for its digital pathology image management system, AISight Dx.