Spryte Medical announced the commencement of enrollment in the INSYTE trial evaluating the company’s neuro-optical CT (nOCT) ...
Otsuka Medical Devices Co., Ltd. and Otsuka Pharmaceutical Co., Ltd., announced the commercial launch of the Paradise ultrasound r ...
CereVasc, Inc. announced results from a prospective, multicenter, single-arm clinical study evaluating the safety and clinical ...
Quantum Surgical, a medical device company specializing in minimally invasive robotic-assisted cancer treatment, announced the ...
Vena Medical, which is based in Canada, announced FDA clearance for the use of its Vena MicroAngioscope system in the peripher ...
Liquet Medical Inc. announced it has received a second FDA 510(k) clearance for a new configuration of its Versus cathete ...
ABK Biomedical, Inc. announced the completion of patient enrollment in the ROUTE90 pivotal study evaluating the company’ ...
Johnson & Johnson MedTech announced the United States launch of the Cereglide 42 and Cereglide 57 aspiration catheters and ...
February 24, 2026—iVascular announced the enrollment of the first patient in the FENCO clinical study evaluating the company’s iCover ball ...
The 2026 AHA/ACC guidelines introduce a five-tier Acute PE Clinical Category system to stratify severity and guide treatment decisions. Mechanical thrombectomy receives a Class 2a recommendation for ...
A clinical discussion on how the long-term findings of the ZILVERPASS study inform decision-making for challenging ...
How do we take on and resolve vein-related pelvic pain in women? PeVD has been associated with venous-origin chronic pelvic ...
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