Bolton Medical Inc.

5 product lines across 1 device categories: Aortic stent grafts.

From terumoaortic.com, checked November 2026.

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About Bolton Medical Inc.

Bolton Medical Inc. hasn't added a company description yet.

Aortic Stent Grafts (EVAR/TEVAR)

Used in: Endovascular Aneurysm Repair (EVAR)

ProductSizes (FDA GUDID)ModelsMRI
RelayPro Thoracic Stent-Graft System
Endovascular Stent-Graft System
Outer Diameter: 22–46 mm; Catheter Gauge: 19–23 Fr; Length: 90–271 mm2247MR Conditional
RelayPro NBS Thoracic Stent-Graft System
Endovascular Stent-Graft System
Outer Diameter: 22–40 mm; Length: 90–259 mm; Catheter Gauge: 19–22 Fr141MR Conditional
TREO Abdominal Stent-Graft System
Endovascular Stent-Graft System
Outer Diameter: 9–36 mm; Length: 40–163 mm; Catheter Gauge: 13–19 Fr86MR Conditional
Relay Plus Thoracic Stent-Graft System
Endovascular stent-graft system
Outer Diameter: 22–46 mm; Length: 90–250 mm; Catheter Gauge: 22–26 Fr84MR Conditional
Relay Thoracic Stent-Graft with Plus Delivery System
Endovascular stent-graft system
Outer Diameter: 22–46 mm; Catheter Gauge: 22–26 Fr; Length: 90–250 mm82MR Conditional

Sales representatives

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From terumoaortic.com, checked November 2026.

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Frequently asked questions

What devices does Bolton Medical Inc. make?

Bolton Medical Inc. has 5 product lines in our library across 1 device category: Aortic stent grafts.

How do I contact a Bolton Medical Inc. sales representative?

Bolton Medical Inc. has not listed sales representatives on LA Vascular yet. Use the company contact details on this page.

Does LA Vascular sell Bolton Medical Inc. products?

No. LA Vascular is an educational reference. We do not sell devices or quote device prices; contact Bolton Medical Inc. or its representatives to buy.

Where do the Bolton Medical Inc. product sizes come from?

From the FDA Global Unique Device Identification Database (GUDID). Confirm sizes and availability with the instructions for use or the manufacturer.

Product lines, models and sizes are compiled from the FDA Global Unique Device Identification Database (GUDID) and FDA clearance records. Descriptions marked "Provided by the manufacturer" come from the company and are reviewed before publishing.

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