Biopsy needles

EnCor EnCompass

by Bard Peripheral Vascular, Inc.

An assembly of devices intended to be used in conjunction with mammography to insert biopsy devices, typically designated needles, into a breast in order to extract a biopsy of a suspect tumour for diagnostic purposes. It consists of a biopsy unit with needle guides, needles, an examination table, and an integral computer for communicating lesion coordinates. This GMDN code includes stand-alone units as well as units that mount onto an existing mammographic radiographic unit.

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EnCor EnCompass models and sizes

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

Model / catalog no.SizeMRIStatus
ENCPConsole— MR UnsafeAvailable
ENCPDriver— MR ConditionalAvailable
ENCPFS— MR ConditionalAvailable
ENCPST— MR UnsafeAvailable

FDA clearances

  • 510(k) K252681 December 2025

Procedures that use biopsy needles

Frequently asked questions

What is EnCor EnCompass used for?

An assembly of devices intended to be used in conjunction with mammography to insert biopsy devices, typically designated needles, into a breast in order to extract a biopsy of a suspect tumour for diagnostic purposes. It consists of a biopsy unit with needle guides, needles, an examination table, and an integral computer for communicating lesion coordinates. This GMDN code includes stand-alone units as well as units that mount onto an existing mammographic radiographic unit.

Who makes EnCor EnCompass?

EnCor EnCompass is made by Bard Peripheral Vascular, Inc.. It is listed under biopsy needles and systems in our device library.

What sizes does EnCor EnCompass come in?

The FDA device database does not list sizes for EnCor EnCompass. Check the instructions for use or ask a Bard Peripheral Vascular, Inc. representative.

Is EnCor EnCompass MRI safe?

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

Is EnCor EnCompass FDA cleared?

EnCor EnCompass is covered by FDA submission K252681.

How do I contact a Bard Peripheral Vascular, Inc. sales representative?

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