By Editor , 13 October 2026
E2 wins FDA 510(k) clearance for Hēlo PE thrombectomy platform

Menlo Park – October 12, 2026 -- Endovascular Engineering, Inc. (E2) has received U.S. FDA 510(k) clearance for both the Hēlo Thrombectomy System and Hēlo Return, a blood return system the company describes as the first cleared for use with continuous vacuum aspiration.