The U.S. Food and Drug Administration authorizes Abbott’s Libre Duo 10 Day Continuous Dual Glucose-Ketone Monitoring System, described as the first wearable to monitor ketones and glucose together in a single device. The authorization covers people ages 2 years and older with diabetes.

The system measures glucose and ketone levels in the fluid just beneath the skin and transmits readings wirelessly to a compatible smartphone, where users can view values and trends over time. Sources also say it can provide alerts if ketone levels reach a concerning threshold. The FDA notes that ketone information should be interpreted alongside glucose readings and symptoms.

Across outlets, the key context is the clinical relevance of ketones: rising ketone levels can indicate risk for diabetic ketoacidosis (DKA), a serious complication that can progress quickly. Reporting also emphasizes that, prior to this type of integrated wearable, ketone monitoring often relied on separate tests that provide single time-point measurements and do not show whether ketones are rising or falling, potentially limiting earlier warning.