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.

Surmodics said that to its knowledge, the threat actor had not released any of its data or used it for any fraudulent purposes. Surmodics has revealed that it is still recovering after it was hit by a ...

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).

Molecular diagnostics company Seegene has launched STAgora, a platform designed for infectious disease analytics.

It is no secret that the UK’s National Health Service (NHS), like many other healthcare systems, is under pressure on multiple fronts. The recent Darzi report, an independent investigation of the ...

US President Donald Trump’s One Big Beautiful Bill Act (H.R. 1) has narrowly passed after US Vice President JD Vance broke a 50-50 deadlock in the US Senate.

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

Field Medical has closed a $35m series B financing round for advancing the development of the FieldForce Pulsed Field Ablation platform.

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