U.S company, FlowAid Medical Technologies Corp., has received CE mark approval for its FA100 SCCD Sequential Contraction Compression Device.
Vascular
CE Mark for Ellipsys® Vascular Access System
Vascular Access specialist Avenu Medical gains European approval and closes in on U.S.
FDA Approval for GORE® EXCLUDER® Iliac Branch Endoprosthesis
Gore-designed all-in-one system to preserve iliac artery blood flow in patients with iliac or aortoiliac aneurysms
US Launch for Nipro’s Cronus™ HP 0.035″ OTW PTA Balloon Catheter
Nipro targets the most resilient stenoses with its new PTA system
First-in-Man Use of AortaFit Fenestrated EVAR System
If the anatomy demands an EVAR graft with sidebranch holes, then 3D printing can seemingly deliver it
New Gore RELINE MAX Study Aims to Confirm Endoprosthesis Benefit in Failed Stenting Patients
108 patient trial will add evidence for treatment of in-stent restenosis using the GORE® VIABAHN® Endoprosthesis
FDA Approval And CE Mark for Boston Scientific’s DVT Catheter
ZelanteDVT catheter is the first AngioJet catheter designed specifically to treat DVT
New Drug-Coating Technology Gets Green Light for Balloon Trial
SurModics receives FDA IDE approval for early feasibility study of the SurVeil™ drug-coated balloon
Cook’s Zenith Alpha™ Thoracic Endovascular Graft Gains FDA Approval
Cook claims its Thoracic Endograft will allow physicians to treat more patients with TEVAR
Lombard Medical Acquires Endovascular Stent Graft Developer Altura Medical
Lombard says the acquisition expands its product portfolio with the addition of Altura’s ultra-low profile endo stent graft
Data Supports Adhesive for Chronic Venous Insufficiency
12 month closure rates for the VenaSeal™ closure system comparable to radiofrequency ablation
3D Helical Stent Study Sees First Patient
Veryan Medical’s helical stent promises much, based as it is on sound physiological principles. They’ll hope IDE study will provide clinical confirmation
FDA Clears Penumbra’s ACE64 Thrombectomy System for Stroke Treatment
Latest mechanical thrombectomy device delivers higher revascularization rates, reduced procedure time and cost
CE Mark of Perivascular Alcohol Denervation System for Hypertension
CE Mark of the Ablative Solutions Peregrine System™ Infusion Catheter signals continued interest in renal denervation therapy
Australian Approval for GORE® EXCLUDER Iliac Branch Endoprosthesis
Gore’s newly approved device builds on its Excluder family of AAA treatment devices and is the first dedicated for use in the common iliac artery
GORE® TAG® Thoracic Branch Endoprosthesis Early Feasibility Study Sees First Patient
US-based study will assess the treatment of aortic arch aneurysms in which perfusion of the brachiocephalic or left common carotid artery is maintained through a branch device