MatOrtho’s ReCerf hip resurfacing arthroplasty (HRA) has secured the CE mark, signifying its adherence to European safety standards.

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.

A new podcast series from industry experts Alleima explores the past, present, and future of the medical device industry.

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 ...