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Terumo Aortic announces commercial launch of TREO Abdominal Stent Graft System in the United States

Following approval this year by the US Food and Drug Administration (FDA) of the TREO® Abdominal Aortic Stent-Graft System for the treatment of patients with abdominal aortic aneurysms (AAA), Terumo Aortic announced today the commercial launch of this endovascular device.

Terumo Aortic announces US FDA Approval for TREO endovascular device

Terumo Aortic today announced that the US Food and Drug Administration (FDA) has granted approval of the TREO® Abdominal Aortic Stent-Graft System for sale in the United States for the treatment of patients with abdominal aortic aneurysms (AAA).

Terumo Aortic Announces US FDA Breakthrough Device designation for Thoraflex Hybrid device

Terumo Aortic today announced that the US Food and Drug Administration (FDA) has granted Breakthrough Device Designation for its innovative Thoraflex Hybrid stented device for complex aortic arch repair.



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Carrie White
Head, Global Marketing Communications
+44 (0) 141 812 5555