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The company named Chad Spooner CFO of MiniMed ahead of plans to spin out the diabetes unit into a separate public firm.
Glucotrack, which is developing a glucose monitor that is implanted through a minimally invasive surgery, said the small ...
Patients whose atrial fibrillation lasts longer than seven days and who do not respond well to drug therapy are now eligible ...
CEO, ATS Corporation. Baxter has appointed Andrew Hider as president and CEO, filling a vacancy created by the retirement ...
Dive Brief: A bankruptcy judge approved the sale of 23andMe to a nonprofit led by Anne Wojcicki, co-founder and former CEO of the genetic testing company. U.S. Bankruptcy Judge Brian Walsh issued an ...
Dive Brief: Intuitive Surgical on Wednesday said its da Vinci 5 robot received CE mark approval for adult and pediatric use in Europe across multiple minimally invasive procedures, including urologic, ...
The launch of the first over-the-counter glucose sensors last year has raised a debate about who benefits from these devices. The Food and Drug Administration cleared devices made by Dexcom and Abbott ...
Diabetes technology companies shared plans for their upcoming devices this weekend at the American Diabetes Association’s Scientific Sessions. Several firms — including Medtronic, Tandem Diabetes Care ...
Tandem Diabetes Care announced new integrations and gave an update on its planned patch pumps at the American Diabetes Association’s Scientific Sessions last weekend. The diabetes tech firm said on ...
The European Commission said late last week it will exclude Chinese suppliers from participating in government purchases of medical devices worth more than 5 million euros ($5.8 million). In addition, ...
Dive Brief: A problem with Dexcom’s receivers for its glucose sensors may cause people to not get an audible alert for low or high blood sugar levels, the Food and Drug Administration said in an ...
Dive Brief: The Food and Drug Administration has blocked certain Olympus Medical devices from entering the U.S. because of quality system failings at a site in Japan. FDA officials issued the import ...
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