Atherectomy
Auryon
A sterile, flexible tube intended to be connected to an atherectomy laser system to invasively direct and deliver laser energy into the peripheral vasculature for the intraluminal photoablation or debulking of lesion material (blockages or total occlusions), to re-establish blood flow within the vessel. It typically consists of fibreoptic materials with a laser-firing distal end and may be designed for over-the-wire (OTW) or rapid exchange insertion. This is a single-use device.
Auryon models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| EXM-2002-1000 | — | Not stated | Available |
FDA clearances
- 510(k) K260244 April 2026
Procedures that use atherectomy
Frequently asked questions
What is Auryon used for?
A sterile, flexible tube intended to be connected to an atherectomy laser system to invasively direct and deliver laser energy into the peripheral vasculature for the intraluminal photoablation or debulking of lesion material (blockages or total occlusions), to re-establish blood flow within the vessel. It typically consists of fibreoptic materials with a laser-firing distal end and may be designed for over-the-wire (OTW) or rapid exchange insertion. This is a single-use device.
Who makes Auryon?
Auryon is made by Eximo Medical Ltd. It is listed under atherectomy devices in our device library.
What sizes does Auryon come in?
The FDA device database does not list sizes for Auryon. Check the instructions for use or ask a Eximo Medical Ltd representative.
Is Auryon MRI safe?
The FDA device database entry for Auryon does not state its MRI safety status. Check the labeling before MRI.
Is Auryon FDA cleared?
Auryon is covered by FDA submission K260244.
How do I contact a Eximo Medical Ltd sales representative?
Eximo Medical Ltd has not listed representatives on LA Vascular yet. Visit the Eximo Medical Ltd company page for contact details.
Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.