Stryker beat Wall Street estimates for fourth-quarter profit and forecast 2025 earnings largely above expectations on Tuesday, fueled by strong demand for its medical and surgical devices.

The US Food and Drug Administration (FDA) has granted 510(k) clearance for Imperative Care’s Zoom System, marking an ...

Among the wave of guidance documents issued by the U.S. Food and Drug Administration (“FDA” or the “Agency”) in the first week of 2025 were ...

Neuralink’s brain-computer interface technology also has been discussed for other potential uses, for example, in mental ...

The website changes raise concerns about “the interference of politics with the study and the practice” of science and ...

Valencia-based Avita Medical Inc. has received FDA approval for a version of its second-generation Recell skin cell ...

If you have a microcurrent device on your wishlist, here are some benefits and drawbacks to consider before you buy one.

NeurAxis offers FDA-cleared IB-Stim device for pediatric IBS pain. Despite positive advancements, market recognition lags.

The U.S. Food and Drug Administration has pulled draft guidance from its website requiring companies to test medicines and ...

Brenner, who worked in the FDA’s Center for Devices and Radiological Health, will take the helm of the agency until a new ...

Dr. Sara Brenner has been named acting commissioner of the Food and Drug Administration. Brenner replaces Dr. Robert Califf. The announcement was made ...

The volume of U.S. FDA warning letters to device makers oscillated significantly in recent years, but the agency posted a handful of these letters to kick off the new year. Five letters were posted ...