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Breast Imaging · GE HEALTHCARE

Invenia ABUS 2.0

See what mammography can miss.

Automated breast ultrasound designed specifically for supplemental screening in dense breast tissue, where mammography alone is not enough.

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Invenia ABUS 2.0

It’s a milestone in the making. Not the end of a path, but the continuation of a journey. Because, like you, we don’t just hope for a healthier future. We insist on creating it.

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Technical Data

Details and Specifications

Invenia ABUS 2.0 was the first FDA-approved ultrasound supplemental screening system designed specifically for detecting cancer in dense breast tissue. Over 40% of women have dense breast tissue, which can mask tumours and limit mammographic performance; mammography may miss more than a third of cancers in dense breasts, and dense tissue itself raises the likelihood of developing cancer several times over. Published data show screening with ABUS increased the relative cancer detection rate by 57% while keeping the recall rate almost stable at 2.3%. The system combines the ABUS 2.0 cSound Imageformer, intelligent imaging algorithms, one-button automation with an icon-driven touchscreen, the Reverse Curve transducer, the Invenia ABUS Viewer and AI Assistant capability.

– First FDA-approved supplemental screening ultrasound for dense breasts
– Invenia ABUS 2.0 cSound Imageformer
– Intelligent imaging algorithms
– One-button automation, icon-driven touchscreen
– Reverse Curve transducer
– Invenia ABUS Viewer
– AI Assistant enabled
– Relative cancer detection rate increase of 57% (published data)
– Recall rate kept almost stable at 2.3%
– Mastery Program, marketing kit and implementation support
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Call us at +355 4 2271385 or email us at Sales@montalshpk.com.

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