Lombard Medical Limited
5 product lines across 1 device categories: Aortic stent grafts.
From lombardmedical.com, checked November 2026.
About Lombard Medical Limited
Lombard Medical Limited hasn't added a company description yet.
Aortic Stent Grafts (EVAR/TEVAR)
Used in: Endovascular Aneurysm Repair (EVAR)
| Product | Sizes (FDA GUDID) | Models | MRI |
|---|---|---|---|
| Aorfix AAA Stent Graft Body with Aorflex Delivery System Aorflex AAA Stent Graft Body with Aorflex Delivery System | — | 602 | MR Conditional |
| Aorfix AAA Stent Graft Plug In Leg with Aorflex Delivery System | — | 42 | MR Conditional |
| Aorfix AAA Stent Graft Distal Extender with Aorflex Delivery System | — | 12 | MR Conditional |
| Aorfix AAA Stent Graft Proximal Extender with Aorflex Delivery System | — | 8 | MR Conditional |
| Aorfix AAA Stent Graft Converter with Aorflex Delivery System | — | 4 | MR Conditional |
Sales representatives
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From lombardmedical.com, checked November 2026.
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FDA clearances and approvals
- aorfix aa flexible stent graft system PMA P110032, 2013
Frequently asked questions
What devices does Lombard Medical Limited make?
Lombard Medical Limited has 5 product lines in our library across 1 device category: Aortic stent grafts.
Are Lombard Medical Limited devices FDA cleared?
Our library lists FDA clearances and approvals for Lombard Medical Limited products. The most recent is aorfix aa flexible stent graft system (PMA P110032, 2013).
How do I contact a Lombard Medical Limited sales representative?
Lombard Medical Limited has not listed sales representatives on LA Vascular yet. Use the company contact details on this page.
Does LA Vascular sell Lombard Medical Limited products?
No. LA Vascular is an educational reference. We do not sell devices or quote device prices; contact Lombard Medical Limited or its representatives to buy.
Where do the Lombard Medical Limited 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.