CAUTION: Investigational Device – Limited by United States law to investigational use. Endospan devices bear the CE marking of conformity.
Endospan Enrolls First Patient in TRIOMPHE IDE Study
FDA Grants NEXUS™ Aortic Arch Stent Graft System Breakthrough Designation
Endospan Enters Into Strategic Distribution Agreement With CryoLife
Endospan elects Jeff Elkins as a Director
Endospan receives CE mark for HORIZON™ EVAR system based on robust clinical and pivotal data to treat Abdominal Aortic Aneurysm (AAA)
Endospan appoints Kevin J. Mayberry as CEO