Product design risks can be mitigated through digital commissioning strategies for device design that speed continuous design ...

AI-powered medical wearables and software are flourishing following the FDA’s new hands-off regulatory guidance.

Small medtech companies can leverage AI without huge investments to compete with major manufacturers using targeted approaches.

WASHINGTON, Dec 22 (Reuters) - Becton Dickinson (BDX.N), opens new tab has been sued by a rival medical device manufacturer for allegedly thwarting competition in the U.S. market for surgical hernia ...

The FDA said it plans to accept new forms of real-world evidence in product applications, starting with a subset of medical device submissions. The agency said the policy change aims to enable the use ...

Dec 9 (Reuters) - Medical device maker Teleflex (TFX.N), opens new tab said on Tuesday it would sell three units for a combined $2.03 billion, as it sharpens its focus on its critical care and ...

Headlines today obsess over tariffs squeezing margins for medical device manufacturers (MDMs). But while tariffs can shave profits, insecure software can obliterate them—and result in patient safety ...

In medical-device software, an update isn’t just a new feature — it can directly affect patient safety. Every code change in a surgical-laser system must be fully traceable to its verification and ...

Take advantage of TipRanks Premium at 50% off! Unlock powerful investing tools, advanced data, and expert analyst insights to help you invest with confidence. Magic ( (MGIC)) has issued an update. On ...

The court concluded that the defendant's duty to defend emergency response systems provider Medical Guardian was triggered because the underlying strict products liability suit brought claims for ...

The FDA released their updated guidance on Cybersecurity in medical devices: Quality System Considerations and content for Premarket submissions at the end of June in 2025. In this guidance the FDA ...