Spotlight Medical, a Paris-based oncology diagnostics company, has announced that myStage Dx has received CE marking under the European Union In Vitro Diagnostic Medical Devices Regulation (IVDR, Regulation (EU) 2017/746).
One paper by Dr. Stuart Turvey and colleagues at BC Children’s Hospital Research Institute (BCCHR) and another paper by Dr. Marie-Claire Arrieta and colleagues from the Snyder Institute for Chronic Diseases and the Alberta Children’s Hospital Research Institute reveal key to treating asthma.
In a study from Karolinska Institutet, the Stockholm3 blood test detected more clinically significant cancer cases than the PSA test, without subjecting more men to unnecessary testing.
A group of researchers from the Technion and the United States reports a breakthrough in MRI scanning in a paper published in Nature Communications.
Researchers at the University of Basel have developed a miniature dental robot that could one day automatically prepare teeth for crowns. The technology could help reduce the number of appointments needed for dental treatment.
Draeger has received FDA 510(k) clearance to market the latest software update for its Evita V800 ventilator. The version 3.10 software release introduces additional features designed to enhance mechanical ventilation for patients with pulmonary conditions, including acute respiratory distress syndrome (ARDS).
The power-injectable implantable port system is designed to support long-term vascular access in adult and paediatric patients.
AorticLab announced today that its FLOWer device received CE mark approval for extended use in transcatheter cardiovascular procedures.
LEM Surgical announced today that the FDA granted a new 510(k) clearance for its Dynamis robotic surgical system.
Masimo, a Danaher (NYSE:DHR) company, today announced FDA clearance for an opioid-induced respiratory depression (OIRD) detection platform.