Avinger, Inc.
3 product lines across 1 device categories: Atherectomy.
From avinger.com, checked November 2026.
About Avinger, Inc.
Avinger, Inc. hasn't added a company description yet.
Atherectomy Devices
Used in: Peripheral Atherectomy
| Product | Sizes (FDA GUDID) | Models | MRI |
|---|---|---|---|
| Pantheris The Pantheris System is intended to remove plaque (atherectomy) from partially occluded vessels in the peripheral vasculature with a reference diameter of… | — | 2 | Not stated |
| Pantheris SV The Pantheris SV System is intended to remove plaque (atherectomy) from partially occluded vessels in the peripheral vasculature with a reference diameter… | — | 1 | Not stated |
| Pantheris LV The Pantheris LV Catheter is a monorail (rapid exchange) device with an effective length of 110 cm, compatible with standard 7F sheaths… | Length: 6–110 cm | 1 | Not stated |
Sales representatives
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From avinger.com, checked November 2026.
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Work for Avinger, Inc.? Add a rep and the areas they cover:
FDA clearances and approvals
- pantheris lv atherectomy catheter 510K K230005, 2023
Frequently asked questions
What devices does Avinger, Inc. make?
Avinger, Inc. has 3 product lines in our library across 1 device category: Atherectomy.
Are Avinger, Inc. devices FDA cleared?
Our library lists FDA clearances and approvals for Avinger, Inc. products. The most recent is pantheris lv atherectomy catheter (510(k) K230005, 2023).
How do I contact a Avinger, Inc. sales representative?
Avinger, Inc. has not listed sales representatives on LA Vascular yet. Use the company contact details on this page.
Does LA Vascular sell Avinger, Inc. products?
No. LA Vascular is an educational reference. We do not sell devices or quote device prices; contact Avinger, Inc. or its representatives to buy.
Where do the Avinger, 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.