Coils

Ruby XL Coil System

by Penumbra, Inc.

A non-bioabsorbable, implantable device intended to induce a thrombosis within a non-neurovascular blood vessel to treat an aneurysm and/or non-neurovascular arteriovenous malformation (AVM); it is not intended for neurovascular application. It is in the form of a metal or metal/synthetic polymer wire which coils upon deployment within an aneurysm or the vasculature surrounding a malformation; it is typically pre-attached to a nonimplantable delivery wire. Disposable devices associated with implantation (e.g., delivery wire, catheter) may be included.

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Ruby XL Coil System models and sizes

From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.

Model / catalog no.SizeMRIStatus
RBYPCXL15-ALength 15 cm MR ConditionalAvailable
RBYPCXL30-ALength 30 cm MR ConditionalAvailable
RBYPCXL45-ALength 45 cm MR ConditionalAvailable
RBYPCXL55-ALength 55 cm MR ConditionalAvailable
RBYPCXL70-ALength 70 cm MR ConditionalAvailable
RBYPODXL0410-ALength 10 cm MR ConditionalAvailable
RBYPODXL0430-ALength 30 cm MR ConditionalAvailable
RBYPODXL0510-ALength 10 cm MR ConditionalAvailable
RBYPODXL0530-ALength 30 cm MR ConditionalAvailable
RBYPODXL0620-ALength 20 cm MR ConditionalAvailable
RBYPODXL0655-ALength 55 cm MR ConditionalAvailable
RBYPODXL0855-ALength 55 cm MR ConditionalAvailable
RBYPODXL0870-ALength 70 cm MR ConditionalAvailable
RBYPODXL1055-ALength 55 cm MR ConditionalAvailable
RBYPODXL1255-ALength 55 cm MR ConditionalAvailable
RBYPODXL1455-ALength 55 cm MR ConditionalAvailable
RBYPODXL1655-ALength 55 cm MR ConditionalAvailable
RBYXL2055-ALength 55 cm MR ConditionalAvailable
RBYXL2455-ALength 55 cm MR ConditionalAvailable
RBYXL2855-ALength 55 cm MR ConditionalAvailable
RBYXL3255-ALength 55 cm MR ConditionalAvailable
RBYXL4055-ALength 55 cm MR ConditionalAvailable
RBYXL4070-ALength 70 cm MR ConditionalAvailable

FDA clearances

  • 510(k) K250079 March 2025

Procedures that use coils

Frequently asked questions

What is Ruby XL Coil System used for?

A non-bioabsorbable, implantable device intended to induce a thrombosis within a non-neurovascular blood vessel to treat an aneurysm and/or non-neurovascular arteriovenous malformation (AVM); it is not intended for neurovascular application. It is in the form of a metal or metal/synthetic polymer wire which coils upon deployment within an aneurysm or the vasculature surrounding a malformation; it is typically pre-attached to a nonimplantable delivery wire. Disposable devices associated with implantation (e.g., delivery wire, catheter) may be included.

Who makes Ruby XL Coil System?

Ruby XL Coil System is made by Penumbra, Inc.. It is listed under embolization coils in our device library.

What sizes does Ruby XL Coil System come in?

Sizes listed for Ruby XL Coil System: Length: 10–70 cm. Confirm availability with the manufacturer's instructions for use.

Is Ruby XL Coil System MRI safe?

The FDA device database lists Ruby XL Coil System as MR Conditional. Always follow the specific MRI conditions in the labeling.

Is Ruby XL Coil System FDA cleared?

Ruby XL Coil System is covered by FDA submission K250079.

How do I contact a Penumbra, Inc. sales representative?

Penumbra, Inc. has not listed representatives on LA Vascular yet. Visit the Penumbra, Inc. 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.

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