InVera Medical Receives FDA Clearance for InVera Infusion Device – a Novel Non-Thermal Catheter for Enhanced Infusion of Sclerosant for Chronic Venous Disease

Encouraging 12-month pilot clinical study results will be presented by Key Opinion Leader Dr. Lowell Kabnick at the prestigious Charing Cross Vascular Symposium in London on Tuesday, April 21st, 2026.

GALWAY, Ireland, April 7, 2026 /PRNewswire/ — InVera Medical, a medical device company focused on advancing minimally-invasive technologies for Chronic Venous Disease, has received FDA 510(k) clearance for the InVera Infusion Device, a new minimally invasive device designed to help physicians deliver treatment more effectively to diseased leg veins, including varicose veins.

Chronic Venous Disease (CVD) affects one in four adults and can progress from visible varicose veins to painful leg ulcers, if left untreated. Despite affecting over 120 million people across the US and Europe, only 1% of those living with venous disease currently receive treatment each year, underlining a significant gap in care that InVera aims to address.

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