Legacy medical devices face growing scrutiny as regulators push for stronger cybersecurity, transparency and risk management.

In a member webinar hosted by techUK, experts from the Medicines and Healthcare products Regulatory Agency (MHRA) provided a comprehensive introduction to the UK’s regulatory framework for software as ...

This medical technology firm delivers integrated blood management solutions to healthcare providers and plasma centers ...

Learn the essential criteria for medical device commercialization in 2026, from AI to global compliance and market trends.

Iran vs US-Israel war: A major US medical device maker, Stryker, has recently faced a cyberattack and investigators are ...

Medical device cyber challenges are among the most complex for manufacturers and healthcare delivery organizations for a variety of reasons, but there are some ...

Automatic scribes run by artificial intelligence now routinely "listen in" on your visit to the doctor. These software ...

Neuracle’s BCI product has assisted patients in regaining the ability to grab and hold objects with their hands.

eyonis® LCS commercial launch is ongoing in U.S. following FDA 510(k) clearance CE-marking regulatory process is on-going with a decision expected in Q2 2026 that could trigger commercial rollout of ...

More than 5,500 Stryker employees in Ireland felt the impact after a major Stryker cyber attack shut down systems at its Cork ...

SOPHIA ANTIPOLIS, France--(BUSINESS WIRE)--Regulatory News: Median Technologies (FR0011049824, ALMDT, “Median” or the “Company”), developer of eyonis®, a suite of artificial intelligence (AI)-powered ...

The Xbox Kinect peripheral, a pretty infamous flop as far as video game accessories go, is no longer supported, but it turns ...