Abbott receives FDA authorization for world's first dual glucose-ketone sensing technology for people with diabetes

Abbott received CE Mark approval in Europe for its Esprit BTK System, a dissolvable stent for peripheral artery disease (PAD) below the knee. The system, which delivers everolimus, is designed to open arteries and dissolve over time. Clinical data showed a 48% reduction in repeat procedures compared to balloon angioplasty. Abbott aims to improve treatment options for PAD, a condition affecting 50 million Europeans.

Abbott (ABT) received FDA authorization for its Libre Duo 10 Day, a dual glucose-ketone sensor. The device is the first of its kind and is designed for people aged two and older. Abbott shares closed at $115.82 on 26 August, up 10.86% over 20 trading days. The company plans to launch the product in the US later in 2026, with compatibility for insulin pump systems from Beta Bionics and Sequel Med Tech. Medtronic's MiniMed unit (MMED) is also developing similar technology. Abbott reported $11.16bn

Abbott received CE-mark approval for its 76mm Esprit BTK system to treat chronic limb-threatening ischaemia (CLTI). The longer-length device addresses the need to treat extensive below-the-knee lesions with fewer scaffolds, reducing procedural complexity. Abbott claims it is the only dissolving resorbable scaffold with robust long-term clinical evidence. The company sees this as an advancement for physicians in Europe, offering a solution for complex CLTI cases.

The FDA approved Abbott's Libre Duo 10 Day, the first wearable device to monitor both glucose and ketones continuously. The system, for diabetes patients aged 2+, received De Novo approval after clinical trials. Abbott plans integrations with insulin pumps from Beta Bionics, Sequel Med Tech, Insulet, Tandem Diabetes, and Medtronic by 2027. ABT shares rose 0.32% to $116.30. Analysts note potential competition with DexCom.

Abbott Laboratories (ABT) received FDA authorization for its Libre Duo 10 Day system, a first-of-its-kind dual glucose ketone sensing biowearable for diabetes management. The device continuously tracks both glucose and ketone levels to address diabetic ketoacidosis risks. Abbott plans a U.S. launch, expanding its digital health and diagnostics portfolio. The company has a market cap of about $201.9 billion.

Abbott (ABT) received FDA authorization for its Libre Duo 10 Day system, the first dual glucose-ketone sensor for diabetes management. The device monitors glucose and detects rising ketones, alerting users to potential DKA emergencies. It integrates with Abbott's digital ecosystem and is compatible with leading automated insulin delivery systems. ABT plans a U.S. launch later this year. The stock traded at $115.30 in pre-market.