The FDA has recalled Mercury Medical’s Neo-Tee T-Piece Resuscitator, a gas powered resuscitator intended primarily for ...

Tazbaz was director of the FDA’s Digital Health Center of Excellence for two years, leading key policies on artificial ...

UW Medicine is unveiling an FDA-approved spinal cord therapy in an effort to offer new hope for paralyzed patients.

Initial public offerings from oil-and-gas company Infinity Natural Resources Inc. and medical-device maker Beta Bionics Inc. both rose in their stock markets debut Friday, as they brushed aside losses ...

Last week, the US Court of Appeals for the Fourth Circuit in United States v. Jackson upheld a doctor’s conviction under Section 301(k) of the ...

The Cybersecurity and Infrastructure Security Agency and Food and Drug Administration Jan. 30 released notices warning of ...

The FDA’s framework for AI regulation, while robust for premarket evaluation, would benefit from more specific mechanisms for continuous monitoring of AI performance in diverse real-world settings.

Pharma, biopharma, and medical device makers should watch out for these perennial problems, which include inadequate ...

The backdoor on Contec CMS8000 patient-monitoring devices could allow an IP address at an unnamed university to remotely ...

Vulnerabilities in certain Contec and Epsimed patient monitors can allow people to gain access and potentially manipulate the ...

Arizona State University's selection is a decorated and internationally renowned psychiatrist and innovator of ...

What will the industry face or achieve in 2025? These trends will be critical in medical device cybersecurity.