-

Shape Memory Medical Announces First Patient Treated in the EMBO-Post Market Surveillance Registry in Germany

SANTA CLARA, Calif.--(BUSINESS WIRE)--Shape Memory Medical Inc., developer of shape memory polymer for peripheral and neurovascular markets, announced the first patient treated in Germany as part of the EMBO-Post Market Surveillance Registry, the Company’s prospective, multicenter, registry study of its IMPEDE and IMPEDE-FX Embolization Plugs when used for peripheral vascular embolization.

The patient was treated by Professor Dr. Götz Martin Richter, Chairman of the Clinics for Diagnostic and Interventional Radiology at the Center for Minimally Invasive Medicine, Klinikum Stuttgart, Germany, in cooperation with the Clinic for Vascular Surgery, Endovascular Medicine and Transplant Surgery in the Klinikum Stuttgart. Ted Ruppel, President and Chief Executive Officer of Shape Memory Medical Inc. said, “We would like to congratulate Professor Richter and the clinical study team at Klinikum Stuttgart for the first EMBO-PMS case in Germany. The addition of German sites accelerates our ability to evaluate the IMPEDE and IMPEDE-FX Embolization Plugs in a variety of uses within the peripheral vasculature.”

The EMBO-Post Market Surveillance Registry (EMBO-PMS) initiated at two centers in the United Kingdom and has now expanded to include up to ten centers in Germany, with a goal of treating up to 125 patients. Results thus far in the United Kingdom reflect treatment for conditions including Iliac artery aneurysm, type II endoleak after TEVAR, type Ib endoleak after EVAR, gluteal artery aneurysm, and splenomegaly. “We are pleased to participate in this important study and look forward to the follow-up from our treated patients,” said Professor Richter, Principal Investigator for EMBO-Post Market Surveillance German Registry.

Both the IMPEDE and IMPEDE-FX Embolization Plugs incorporate Shape Memory Medical’s novel shape memory polymer, a porous, radiolucent, embolic scaffold that is crimped for catheter delivery and self-expands upon contact with blood, that enables conversion to organized thrombus followed by gradual healthy tissue formation. Pre-clinical and clinical studies have shown that shape memory polymer offers effective and predictable space filling, stable clot formation for embolization, and progressive healing as the material is absorbed.

“We look forward to collaborating with colleagues from Germany to add to the experience within EMBO-PMS,” said Professor Robert Morgan, Consultant Vascular and Interventional Radiologist, St. George’s NHS Trust, London, UK and Principal Investigator, EMBO-Post Market Surveillance UK Registry. “We’re continuing to obtain data to support the safety and effectiveness of the IMPEDE devices across a variety of peripheral vascular anatomies with technical success and target vessel thrombosis achieved in all cases,” continued Morgan. Preliminary experience in EMBO-PMS is published in CVIR Endovascular 2021 Mar 9;4(1):29.

About Shape Memory Medical

Shape Memory Medical Inc. is dedicated to developing innovative therapeutic solutions with its proprietary shape memory polymers. Neurovascular embolization products include the TrelliX® Embolic Coil, which is CE marked for use in the EU. Peripheral embolization products include the IMPEDE® and IMPEDE-FX Embolization Plugs and IMPEDE-FX RapidFill® Device. In countries recognizing CE marking, the IMPEDE and IMPEDE-FX Embolization Plugs and the IMPEDE-FX RapidFill are indicated to obstruct or reduce the rate of blood flow in the peripheral vasculature. In the United States, the IMPEDE Embolization Plug is indicated to obstruct or reduce the rate of blood flow in the peripheral vasculature, and the IMPEDE-FX Embolization Plug is indicated for use with the IMPEDE Embolization Plug to obstruct or reduce the rate of blood flow in the peripheral vasculature. The IMPEDE and IMPEDE-FX Embolization Plugs are PMDA approved in Japan. The TrelliX Embolic Coil and IMPEDE-FX RapidFill Device are not available in the United States or Japan.

For more information, visit www.shapemem.com.

Contacts

Shape Memory Medical

Details
Headquarters: San Jose, CA
CEO: Edward Ruppel
Employees: 25-50
Organization: PRI

Release Versions

Contacts

Social Media Profiles
More News From Shape Memory Medical

Shape Memory Medical Completes Enrollment in Landmark AAA‑SHAPE Randomized Controlled Pivotal Trial

SAN JOSE, Calif.--(BUSINESS WIRE)--Shape Memory Medical Inc., developer of the only commercially available volume‑expanding shape memory polymer for endovascular embolization, announced today that it has completed enrollment in the AAA‑SHAPE Pivotal Trial, a prospective, multicenter, randomized, open‑label controlled study evaluating the safety and effectiveness of the IMPEDE‑FX RapidFill® Device when used alongside endovascular aneurysm repair, or EVAR, to improve abdominal aortic aneurysm (AA...

Shape Memory Medical Begins Enrollment in FLAGSHIP Study Evaluating Novel False Lumen Embolization Technology

SAN JOSE, Calif.--(BUSINESS WIRE)--Shape Memory Medical Inc., developer of custom shape memory polymers for endovascular applications, today announced enrollment of the first patients in FLAGSHIP, the Company’s prospective, single‑arm, open‑label first‑in‑human study evaluating its investigational False Lumen Embolization (FLE) System for the treatment of aortic dissection. Aortic dissection is a life‑threatening condition in which a tear in the aortic wall creates a secondary channel known as...

Shape Memory Medical Secures EU MDR Certification for IMPEDE® Embolization Plug Product Family, Accelerating Global Innovation in Vascular Care

SAN JOSE, Calif.--(BUSINESS WIRE)--Shape Memory Medical Inc., innovator of the proprietary shape memory polymer technology for endovascular applications, announced that its IMPEDE® Embolization Plug product family has received certification as a Class III device under the European Union (EU) Medical Device Regulation (MDR) 2017/745. The IMPEDE Embolization Plug family, previously CE-marked under the Medical Device Directive 93/42/EEC (MDD), has now earned the more stringent EU MDR certification...
Back to Newsroom