The U.S. Food and Drug Administration (FDA) terminated a recall for Berkeley Club Beverages water on November 13 and ...
Think Surgical announced today that it received FDA 510(k) clearance to use its TMINI surgical robot with the LinkSymphoKnee.
Pharmacies that make customized medications are asking the federal Food and Drug Administration to protect their right to ...
A Vitamin B supplement has been recalled due to being incorrectly formulated with niacin rather than niacinamide.
An FDA advisory committee has unanimously concluded that oral phenylephrine, a decongestant found in many cold and flu ...
The US Food and Drug Administration (FDA) has approved Syndax Pharmaceuticals' Revuforj (revumenib) for treating relapsed or ...
The FDA-cleared Spectral CT 7500 RT, a detector-based computed tomography radiotherapy solution aimed to enhance radiation ...
BrightHeart announced that it received FDA 510(k) clearance for its first AI software for prenatal ultrasound evaluations of ...
The product tested positive for Coliform, which are "considered indicators of fecal contamination and, thus, pathogenic ...
Kennedy has been most vocal about the FDA, an agency that oversees nearly $3 trillion in medicines, food and tobacco products ...
Revuforj is the first so-called menin inhibitor cleared in the U.S., securing FDA approval for use in adults and certain ...