IVC filters

Greenfield

by Boston Scientific Corporation

A permanently implanted vascular device intended to be percutaneously placed in the inferior vena cava (IVC) to prevent pulmonary embolism (PE). The device achieves its unconstrained diameter upon deployment in the IVC and imparts an outward radial force on the luminal surface of the vena cava to ensure proper positioning and stability. It is designed for blood clot capture while maintaining caval patency. It is made of metal alloys [e.g., stainless steel, titanium (Ti), nickel-titanium alloy (Nitinol)] and is available in various self-expanding, wire designs (e.g., conical, basket).

Contact a rep Compare similar devices

Greenfield models and sizes

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

Model / catalog no.SizeMRIStatus
M001503000— MR ConditionalAvailable
M001503010— MR ConditionalAvailable
M001504000— MR ConditionalAvailable
M001505010— MR ConditionalAvailable

Procedures that use ivc filters

Frequently asked questions

What is Greenfield used for?

A permanently implanted vascular device intended to be percutaneously placed in the inferior vena cava (IVC) to prevent pulmonary embolism (PE). The device achieves its unconstrained diameter upon deployment in the IVC and imparts an outward radial force on the luminal surface of the vena cava to ensure proper positioning and stability. It is designed for blood clot capture while maintaining caval patency. It is made of metal alloys [e.g., stainless steel, titanium (Ti), nickel-titanium alloy (Nitinol)] and is available in various self-expanding, wire designs (e.g., conical, basket).

Who makes Greenfield?

Greenfield is made by Boston Scientific Corporation. It is listed under ivc filters in our device library.

What sizes does Greenfield come in?

The FDA device database does not list sizes for Greenfield. Check the instructions for use or ask a Boston Scientific Corporation representative.

Is Greenfield MRI safe?

The FDA device database lists Greenfield as MR Conditional. Always follow the specific MRI conditions in the labeling.

Is Greenfield FDA cleared?

Greenfield is registered in the FDA's Global Unique Device Identification Database (GUDID).

How do I contact a Boston Scientific Corporation sales representative?

Boston Scientific Corporation has not listed representatives on LA Vascular yet. Visit the Boston Scientific Corporation 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.

📬 The IR Device Brief

One email a month: new FDA clearances, recalls and device pages in vascular & interventional radiology.

We'll email you a link to confirm. Unsubscribe any time.

Suggest edits

For manufacturers and their teams. Each field shows what the page says now: add, remove or rewrite anything, and leave the rest as is. LA Vascular reviews every change before it goes live.

About you