Us2.ai

What does Us2.ai do?

Us2.ai is an FDA-cleared AI platform that fully automates echocardiogram analysis — measurements, disease detection, and a structured report generated in seconds from a single DICOM upload. It plugs into existing PACS, CVIS, and reporting systems without changing how studies are acquired.

How is Us2.ai different from other AI echocardiography tools?

Most tools assist with a single task — strain, ejection fraction, or view classification. Us2.ai delivers an end-to-end report covering guideline measurements, diastolic and valvular assessment, and disease screening (cardiac amyloidosis, heart failure, aortic stenosis, pulmonary hypertension) in one zero-click pass. It is vendor-neutral across GE, Philips, Siemens, Canon, and handheld POCUS.

Where is Us2.ai cleared for clinical use?

Us2.ai holds regulatory clearance in 28+ markets including FDA (US), CE MDR (EU), MHRA (UK), TGA (Australia), Health Canada, PMDA (Japan), and HSA (Singapore). See the Regulatory Status page for the full market-by-market list with certificate identifiers.

How long does it take to deploy Us2.ai?

Typical go-live is about one month from kickoff: scoping, install, clinical validation, and production. Cloud deployments are fastest; on-premise installations follow the same four milestones with hospital-IT involvement during install.

Is AI echocardiography reimbursable?

In the US, echocardiography procedures are billed under established Category I CPT codes (e.g. 93306 for complete TTE, 93350 for stress echo). For specific AI-enabled coded indications, CMS has established dedicated codes — for example, Category III code 0932T for AI-derived heart failure with preserved ejection fraction (HFpEF) detection, effective January 1, 2025. See US Reimbursement for codes, Medicare payment methodologies, and OPPS / NTAP detail. Per-country coding and coverage for the UK, Germany, France, Switzerland, Canada, Brazil, Australia, Japan, India, Taiwan, Thailand, Philippine

How accurate is Us2.ai?

Us2.ai's automated measurements have been validated in peer-reviewed studies against expert readers, with agreement at or above inter-reader variability for ejection fraction, GLS, diastolic function, and disease detection endpoints. See Clinical Evidence for the full publication record.

Is patient data safe with Us2.ai?

Yes. Us2.ai is HIPAA and GDPR compliant, ISO 27001:2022 certified, SOC 2 Type II audited, and MDSAP certified. On-premise deployment is available where data must remain inside the hospital network.