Carotid stents
Precise
A non-bioabsorbable tubular device dedicated to implantation in a carotid artery to maintain arterial patency and improve luminal diameter in patients with atherosclerotic disease. It is made of metal [e.g., nickel-titanium alloy (Nitinol)] typically in a tubular mesh structure, and is typically delivered to the site of implantation by a dedicated instrument where it self-expands upon release. It is available in a variety of lengths and diameters and may be used in conjunction with an embolic protection device. Disposable devices associated with implantation may be included.
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Where to buy Precise
Contact Cordis US Corp. directly; they can quote, ship, or point you to the distributor for your country.
From cordis.com, checked October 2026.
No reply, or outside their markets? Send us a request and we route it to a rep or distributor for your country.
FDA clearances
- PMA P030047 April 2016
Procedures that use carotid stents
Frequently asked questions
What is Precise used for?
A non-bioabsorbable tubular device dedicated to implantation in a carotid artery to maintain arterial patency and improve luminal diameter in patients with atherosclerotic disease. It is made of metal [e.g., nickel-titanium alloy (Nitinol)] typically in a tubular mesh structure, and is typically delivered to the site of implantation by a dedicated instrument where it self-expands upon release. It is available in a variety of lengths and diameters and may be used in conjunction with an embolic protection device. Disposable devices associated with implantation may be included.
Who makes Precise?
Precise is made by Cordis US Corp.. It is listed under carotid stents in our device library.
What sizes does Precise come in?
The FDA device database does not list sizes for Precise. Check the instructions for use or ask a Cordis US Corp. representative.
Is Precise MRI safe?
The FDA device database lists Precise as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Precise FDA cleared?
Precise is covered by FDA submission P030047.
How do I contact a Cordis US Corp. sales representative?
Cordis US Corp. has not listed representatives on LA Vascular yet. Visit the Cordis US Corp. 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.