About the Artificial Dye Ban. On April 22, the FDA issued a statement saying it will phase out all petroleum-based synthetic ...

California-based ICU Medical failed to submit proper documents for significant changes to two devices made in Minneapolis, ...

The FDA plans to phase out petroleum-based food dyes, aiming to protect public health—especially children—as part of the ...

The FDA has cleared the Dexcom G7 15 Day continuous glucose monitoring system for individuals 18 years and older with diabetes.

BD (NYSE: BDX) announced today that it received FDA 510(k) clearance for its Phasix ST umbilical hernia patch.

After firing several employees, FDA is planning to hire contractors in place of fired staff. The departed staffers include ...

The contractors would effectively replace most of the work done by more than 50 laid-off federal employees who handled travel ...

ICU Medical Inc, a worldwide leader in the development, manufacture and sale of innovative medical devices, has announced 510(k) regulatory clearance from the US Food and Drug Administration (FDA) for ...

An FDA approval is a hard-won milestone allowing a medtech company to widely commercialize life-changing technology and set guidance for future financial performance. It can take years for the ...

“As a buyer or consumer, you need to ensure that every supplement you purchase is regulated by the FDA (Food and Drugs Authority). And you shouldn't rely solely on the stamp or label ...

The FDA approved the use of Opdivo with Yervoy in front-line colorectal cancer, while a Manhattan court junked a class action complaint over the blood cancer drug Pomalyst. Tuesday was a good day for ...