Treating a wider range of patients1-9
The VBX Stent Graft has the broadest range of on-label indications1–9:
| Iliac occlusive | Coarctation of the aorta | Aortic bifurcation | De novo or restenotic visceral arteries | Iliac aneurysm | Visceral aneurysm | Subclavian aneurysm | Trauma/injury | Fistula | Fenestrated endovascular aortic repaira,b | Branched endovascular aortic repaira,b | |
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| GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis¹ | √ |
| √ | √ | √ | √ | √ | √ | √ | √ | √ |
| GETINGE ADVANTA® V12® Balloon Expandable Covered Stent² | √ |
| √ | Renal only (5-7 mm) |
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| BENTLEY® BEGRAFT® Peripheral Stent Graft System³ | √ |
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| Renal only | √ | Renal only |
| √ | √ | √ |
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| BENTLEY® BEGRAFT® Peripheral PLUS Stent Graft System⁴ | √ |
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| Renal only | √ | Renal only |
| √ | √ |
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| BENTLEY® BEGRAFT® Aortic Stent Graft System⁵ | √ | √ |
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| BENTLEY® BEFLARED® FEVAR Stent Graft System⁶ |
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| BENTLEY® BEFLOW® Iliac Covered Stent System⁷ | √ |
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| BD® LIFESTREAM® Balloon Expandable Vascular Covered Stent⁸ | √ |
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| IVASCULAR® ICOVER® Balloon Expandable Covered Stent System⁹ | √ |
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| Renal only | √ | Renal only |
| √ | √ |
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VBX Stent Graft – MDR approved in all listed indications.
Deliver customized treatment with the VBX Stent Graft.
a This indication requires the devices to be used in conjunction with an aortic main body, and the intent of the indication is to provide perfusion to visceral vessels.
b Not applicable to Reduced Profile GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis (BXB catalogue numbers).
- Gore Medical Products Instructions for Use (IFU). W. L. Gore & Associates, Inc. Accessed July 26, 2025. https://eifu.goremedical.com/
- Advanta V12 Balloon Expandable Covered Stent [Instructions for Use]. Atrium Medical Corporation; 2019. AW011076. Rev AB.
- BeGraft Peripheral Stent Graft System [Instructions for Use]. Bentley InnoMed GmbH; 2018.
- BeGraft Peripheral Plus Stent Graft System [Instructions for Use]. Bentley InnoMed GmbH; 2019. #401797-001/005.
- BeGraft Aortic Stent Graft System [Instructions for Use]. Bentley InnoMed GmbH; 2016.
- BeFlared FEVAR Stent Graft System [Instructions for Use] Bentley InnoMed GmbH; 2024. 406725-001e/002.
- BeFlow Iliac Covered Stent System [Instructions for Use] Bentley InnoMed GmbH; 2024. 404742-001e/002.
- LifeStream™ Balloon Expandable Vascular Covered Stent [Instructions for Use]. Clearstream Technologies, Ltd; 2020. PK1299800. Rev. 5. 05/20.
- iVascular® iCover Balloon Expandable Stent System [Instructions for Use]. iVascular S.L.U.; 2021. MP45030 Ed.0. March 2021.
Refer to Instructions for Use at eifu.goremedical.com for a complete description of all applicable indications, warnings, precautions and contraindications for the markets where this product is available. RXOnly
INDICATIONS FOR USE IN EUROPE: The GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis is indicated for the treatment of:
- de novo or restenotic lesions found in iliac arteries, including lesions at the aortic bifurcation;
- de novo or restenotic lesions in the visceral arteries;
- isolated visceral, iliac, and subclavian artery aneurysms; or
- traumatic or iatrogenic vessel injuries in arteries that are located in the chest cavity, abdominal cavity, or pelvis (except for aorta, coronary, innominate, carotid, vertebral, and pulmonary arteries).
The GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis is indicated for use as a bridging stent in branched and fenestrated endovascular aortic aneurysm repair with the followingb:
- Approved for use branched aortic endovascular grafts constructed of polyester fabric, stainless steel stents, and polypropylene suture with branch diameters of 6/8 mm and lengths of 18/21 mm.
- Approved for use fenestrated aortic endovascular grafts constructed of polyester fabric, stainless steel stents, and fenestrations with polypropylene suture ranging in diameter from 6–8 mm.
CONTRAINDICATIONS: Do not use the GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis in patients with known hypersensitivity to heparin, including those patients who have had a previous incident of Heparin-Induced Thrombocytopenia (HIT) type II.