One-year results from IVC stent clinical trial show positive safety and efficacy data

Twelve-month results from the clinical trial assessing a dedicated venous stent for the treatment of symptomatic inferior vena cava (IVC) obstruction with or without combined iliofemoral obstruction showed the device exceeded its performance goal for freedom from a composite of…
TAMBE and TBE: Evolving experiences and piecing together channels of inquiry

New findings chronicling progress with both the Gore Excluder thoracoabdominal branch endoprosthesis (TAMBE)— approved by the Food and Drug Administration (FDA) last year—and Gore Tag thoracic branch endoprosthesis (TBE), which recently acquired a new indication for use in aortic zones…
MVSS 2025: Gore iliac branch device ‘equally effective’ in both IDE and registry studies

Researchers have reported comparable five-year outcomes of the Gore Excluder iliac branch endoprosthesis (IBE; Gore) in both the investigational device exemption (IDE) and GREAT registry studies of the device. Meghan Barber, MD, a vascular surgery fellow at the University of…
Gore announces MDR expanded indication for the Viabahn VBX balloon-expandable endoprosthesis as a bridging stent

Gore today announced CE-mark approval of an expanded indication for the Gore Viabahn VBX balloon-expandable endoprosthesis (VBX stent graft) when used as a bridging stent with branched and fenestrated aortic endografts in the treatment of aortic aneurysms involving the renal…
Gore Tag thoracic branch endoprosthesis receives expanded FDA approval for endovascular aortic arch repair

Gore has announced that the Gore Tag thoracic branch endoprosthesis (TBE) is now approved by the Food and Drug Administration (FDA) for use in Zones 0 and 1, expanding its indication for the endovascular repair of lesions in the aortic…
Gore announces FDA approval and first commercial implant of large-diameter thoracic tapers

Gore recently announced the expansion of the Gore Tag conformable thoracic stent graft with Active Control system product line, following Food and Drug Administration (FDA) approval of four new large-diameter tapered designs: 34x28mm, 37x31mm, 40x34mm and 45x37mm. News of the…
SCVS 2025: TBE device provides ‘safer’ option than TEVAR for blunt thoracic injuries in setting of zone 2 coverage

Use of the Gore Tag thoracic branch endoprosthesis (TBE) “offers a safer alternative” to traditional thoracic endovascular aortic repair (TEVAR) with left subclavian artery (LSA) coverage in blunt thoracic aortic injury (BTAI) requiring zone 2 coverage for zone 2 or…
Gore announces first commercial implant of Excluder conformable AAA endoprosthesis with Active Control system in Canada

Gore recently announced the first commercial use of its Excluder conformable abdominal aortic aneurysm (AAA) endoprosthesis with Active Control system in Canada. The news coincides with Health Canada approval of the device for the treatment of AAA patients with aortic…
Gore receives CE mark for lower profile Viabahn VBX endoprosthesis

Gore has announced recent CE mark of a lower profile Viabahn VBX balloon expandable endoprosthesis (VBX stent graft). Medical Device Regulation (MDR) approval of this innovation builds on a proven device which has become an important tool for treating complex…
Hybrid aortic arch: ‘We believe there is still a role for a versatile multiple-branched arch option’

Mid-term results from an analysis of a series of hybrid aortic arch reconstructions utilizing overlapping single thoracic branch endoprostheses in a dual-branch configuration showed the technique to be safe and versatile. Delivered at the 2024 Western Vascular Society (WVS) annual…

