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Pounce Thrombus Retrieval System Receives FDA Approval – Non-Surgical Removal of Thrombi and Emboli from the Peripheral Arterial Vasculature

The Pounce Thrombus Retrieval System is intended for the non-surgical removal of thrombi and emboli from the peripheral arterial vasculature.

SurVeil™ Drug Coated Balloon Receives CE Mark

The SurVeil DCB, a next-generation device that utilizes best-in-class technology in the treatment of peripheral artery disease (PAD), includes a proprietary drug-excipient formulation for a durable balloon coating and is manufactured using an innovative process to improve coating uniformity.

4/23/19: Surmodics Sublime Guide Sheath Receives FDA 510(k) Approval

The highly flexible, proprietary Xtreme® braid-reinforced Sublime guide sheath is designed to resist kinking and maximize strength while retaining a low profile. The sheath will be available in 5Fr and 6Fr diameters, and 120cm and 150cm lengths.

FDA Clearance of a New .018” Low-Profile PTA Balloon Dilation Catheter Reported by Surmodics

4/23/18: The company reports continued progress in R&D whole-product solutions pipeline.

Surmodics Reports Second Quarter Fiscal 2017 Results, Updates Fiscal 2017 Financial Guidance

"This was an excellent quarter, both in terms of our revenue performance above expectations and the progress...

Surmodics Appoints Lisa Wipperman Heine to Its Board of Directors

Surmodics provides surface modification technologies for intravascular medical devices and a leading provider of chemical components for...