Diabeloop receives FDA 510(k) clearance for DBLG2, an Automated Insulin Delivery algorithm in an App
Diabeloop receives FDA 510(k) clearance for DBLG2, an Automated Insulin Delivery algorithm in an App: a strategic ...
In a pair of guidance documents released Tuesday, the regulator clarified the types of wellness features and clinical ...
“FDA’s proposed rule, ‘Use of Formaldehyde and Formaldehyde-Releasing Chemicals as an Ingredient in Hair Smoothing Products ...
Certain people risk severe or life-threatening reactions if they consume these products, according to an official alert.
The FDA classification underscores the urgency of the situation and the potential danger posed by the contaminated products.
Former FDA Commissioner Dr. Scott Gottlieb joins 'Squawk Box' to discuss the ongoing research and efforts at the FDA to find ...
MedPage Today on MSN
FDA Flags Medtronic Recall as Most Serious; Hep B Cure? Appendectomy for UC
The FDA designated the recall of certain Medtronic Bravo esophageal pH monitoring capsules as class I, the most serious type.
FDA plans limited regulation of wearable medical devices, boosting Apple, Fitbit, Oura stocks as 50% of Americans use fitness ...
The Food and Drug Administration (FDA) updated its guidance on Tuesday to allow more wearables to fall into a general ...
SAN FRANCISCO, CALIFORNIA / ACCESS Newswire / January 2, 2026 / Jaguar Health, Inc. (NASDAQ:JAGX) ("Jaguar") today ...
GlobalData on MSN
Octapharma receives FDA approval for new Fibryga formulation in AFD
Octapharma has received approval from the US Food and Drug Administration (FDA) for a new 2-gram (g) formulation of Fibryga ...
January 2026 Consumer Report Examines How PeterMD and Similar Platforms Facilitate Prescription Hair Loss Treatment Access ...
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