FDA announces wearable devices providing non-medical info won't face regulation, offering clarity on digital health technology and AI policies.

On January 6, 2026, the US Food and Drug Administration (FDA) revised its final guidance on Clinical Decision Support ...

In a pair of guidance documents released Tuesday, the regulator clarified the types of wellness features and clinical ...

FDA plans limited regulation of wearable medical devices, boosting Apple, Fitbit, Oura stocks as 50% of Americans use fitness ...

The FDA will ease regulation of digital health products, aiming to deregulate AI and promote its widespread use.

On January 6, 2026, the U.S. Food and Drug Administration (“FDA”) published revised final guidance documents on Clinical Decision Support ...

These technologies are improving all the time. If they’re not making claims that they are medical grade, let’s let the market decide” says FDA boss ...

FDA commissioner Marty Makary revealed at the 2026 CES trade show in Las Vegas that low-risk devices will face less regulatory oversight.

Woori IO plans to accelerate its noninvasive CGM launch after FDA announced relaxed wearable device regulations.

FDA’s decision to limit regulations of non-medical grade wearables marks a notable shift toward regulatory restraint in digital health. FDA announced its plan to stop subjecting non-medical grade ...

A recently released analysis report from the Deloitte Center for Government Insights that examines the US’s current and proposed software as a medical device (SaMD) regulatory landscape, and includes ...

DUBLIN--(BUSINESS WIRE)--The "Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations" conference has been added to ResearchAndMarkets.com's offering. This intensive four-day ...