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June 25, 2026
SKYWARD Pivotal Studies of Shockwave SkyRunner Carotid IVL Platform Begin Enrollment
June 25, 2026—Johnson & Johnson announced the initiation of its SKYWARD investigational device exemption (IDE) clinical program evaluating the company’s Shockwave SkyRunner carotid intravascular lithotripsy (IVL) system for the treatment of calcified carotid arteries when used before stenting with a commercially available transcarotid or transfemoral stent system.
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News | June 25, 2026Jun252026
News | June 24, 2026Jun242026
STRIDE Pivotal Trial of CereVasc’s eShunt System Completes Enrollment
June 24, 2026—CereVasc, Inc. announced it has completed patient enrollment in the STRIDE pivotal trial, which is evaluating the company’s investigational eShunt system in patients with normal pressure hydrocephalus (NPH).
News | June 23, 2026Jun232026
ESVS Focused Update of PAD Guidelines Addresses Safety Concerns of Paclitaxel
June 23, 2026—The European Society of Vascular Surgery (ESVS) announced the publication of a focused update on the ESVS peripheral artery disease (PAD) guidelines addressing the new findings on the safety of paclitaxel-coated devices.
Cook’s Volante Steerable Guiding Sheath Launched in United States
June 23, 2026—Cook Medical announced that the Volante steerable guiding sheath is now commercially available in the United States and select global markets.
Access Vascular and Medline Partner on Commercialization of Cobranded Vascular Access Catheters
June 23, 2026—Access Vascular, Inc. (AVI) and Medline announced a multiyear agreement to accelerate the rollout of AVI’s next-generation catheters, the HydroMid and HydroPICC.
News | June 22, 2026Jun222026
Route 92’s Neurovascular Portfolio Approved in Canada
June 22, 2026—Route 92 Medical, Inc. announced that the first commercial cases in Canada were performed with the company’s neurovascular devices.
News | June 19, 2026Jun192026
SYMPHONY-PE Analysis Shows Early Thrombectomy Linked to Better Outcomes
June 19, 2026—Imperative Care announced findings from a post hoc analysis of the SYMPHONY-PE trial that suggest that mechanical thrombectomy performed within 12 hours of diagnosis may be associated with greater hemodynamic and right ventricular recovery in patients with intermediate-risk pulmonary embolism (PE) compared with treatment performed later.
News | June 16, 2026Jun162026
ThruFlo Secures Funding to Advance Development of Its Flow Diverter for Bifurcation Aneurysms
June 16, 2026—ThruFlo Endovascular, Inc., a neuroendovascular medical device company, announced the completion of seed funding to accelerate development of its bifurcated flow diverter platform.
New Directions in Neurointervention
Key trials, new guidelines, and emerging therapies.
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May 5, 2026
Solaris DE Drug-Eluting Covered Stent Receives FDA Breakthrough Device Designation
February 9, 2026
DISTALS Results Presented for Rapid Medical Tigertriever 13 in MVO Stroke
April 13, 2026
Stryker to Acquire Amplitude Vascular Systems