Peripheral stents
S.m.a.r.t. Radianz
A non-bioabsorbable tubular device intended to be implanted in a peripheral artery (excludes aorta, coronary, pulmonary, and intracranial arteries) to indefinitely maintain patency and improve luminal diameter in patients with atherosclerotic disease, or following the recanalization of a total occlusion. It may additionally be intended to be implanted in an obstructed biliary duct; it is not dedicated to carotid artery implantation, and not intended for connection with an aortic stent. It is made entirely of metal [e.g., Nitinol alloy mesh structure] and typically implanted by a dedicated instrument where it self-expands upon release or is balloon expanded.
FDA clearances
- PMA P020036 January 2026
- PMA P120002 September 2025
Procedures that use peripheral stents
Frequently asked questions
What is S.m.a.r.t. Radianz used for?
A non-bioabsorbable tubular device intended to be implanted in a peripheral artery (excludes aorta, coronary, pulmonary, and intracranial arteries) to indefinitely maintain patency and improve luminal diameter in patients with atherosclerotic disease, or following the recanalization of a total occlusion. It may additionally be intended to be implanted in an obstructed biliary duct; it is not dedicated to carotid artery implantation, and not intended for connection with an aortic stent. It is made entirely of metal [e.g., Nitinol alloy mesh structure] and typically implanted by a dedicated instrument where it self-expands upon release or is balloon expanded.
Who makes S.m.a.r.t. Radianz?
S.m.a.r.t. Radianz is made by Cordis US Corp.. It is listed under peripheral artery stents and covered stents in our device library.
What sizes does S.m.a.r.t. Radianz come in?
Sizes listed for S.m.a.r.t. Radianz: Length: 150–190 cm. Confirm availability with the manufacturer's instructions for use.
Is S.m.a.r.t. Radianz MRI safe?
The FDA device database lists S.m.a.r.t. Radianz as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is S.m.a.r.t. Radianz FDA cleared?
S.m.a.r.t. Radianz is covered by FDA submissions P120002, P020036.
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.