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VENITI is dedicated to providing innovative technologies for the treatment of venous disease.


The VICI VENOUS STENT® System is the first stent designed from inception for use in the venous system. The stent is designed to provide high crush resistance, end-to-end strength and shape with flexibility, and controlled deployment. Since receiving CE marking for the VICI VENOUS STENT® System, in October 2013, VENITI has achieved several important milestones. The product is currently available for commercial use in the European Union, and has received an Investigational Device Exemption (IDE) approval in the United States. VENITI began U.S. clinical trial procedures in the Fall of 2014.



The VENITI VICI VENOUS STENT® System is CE marked under the European Medical Devices Directive (93/42/EEC) and commercially available in Europe. CAUTION: Investigational device. Limited by United States law to investigational use.