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Edwards Lifesciences has recalled over 61,000 units of its OptiSite Arterial Cannula and FEM-Flex II Femoral Arterial Cannula due to a potential safety hazard, according
Route 92 Medical reported positive outcomes from a retrospective multicenter study of its FDA-cleared HiPoint 88 reperfusion system for acute ischemic stroke. The HiPoint 88
The FDA has approved Bayer’s finerenone (Kerendia), a non-steroidal mineralocorticoid receptor antagonist (MRA), for patients with heart failure and left ventricular ejection fraction (LVEF) ≥40%.
Siemens Healthineers’ Varian announced the CE marking and European launch of its IntelliBlate microwave ablation system for image-guided cancer therapy. The system received FDA clearance