Last updated: May 25, 2026

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Koios DS Breast medical AI product profile

Smart ultrasound software that analyzes breast ultrasound images and supports physician risk assessment for suspicious lesions.

Screenshot of the official Koios DS Breast product page
Medical imaging and radiology

Best fit

Breast ultrasound teams evaluating adjunctive CADx support while preserving trained physician interpretation and BI-RADS workflow responsibility.

Primary use case
AI-assisted risk assessment and computer-aided diagnosis support for breast ultrasound lesions
Audience
Breast imaging centers, diagnostic radiology groups, ultrasound clinics, and health systems using breast ultrasound
Risk level
High
Pricing signal
Enterprise and provider pricing; verify current module, thyroid/breast scope, billing workflow, and deployment terms.
Official sources
4 official sources

Compare within workflow: Medical imaging and radiology · comparison shortlist · source index

Regulatory, privacy, evidence, and workflow lens

product-specific source-backed lens: These product-specific signals summarize what the cited sources imply before treating Koios DS Breast as safe for a local clinical, operational, or research workflow.

Regulatory / FDAMatch K212616 or the relevant current clearance to the exact breast ultrasound workflow, patient group, lesion type, and trained interpreting-physician use.
PrivacyReview ultrasound image transfer, DICOM metadata handling, cloud or local processing, retention, user access, audit logs, and security documentation before sending clinical studies.
EvidenceValidate CADx performance on local ultrasound equipment, operator mix, lesion prevalence, benign/malignant balance, subgroup representation, and downstream biopsy decisions.
WorkflowBest used as adjunctive physician-reviewed ultrasound decision support, with explicit documentation of ROI selection, AI output review, BI-RADS reconciliation, and final clinician accountability.

Where Koios DS Breast fits

Koios describes Koios DS Breast as FDA-cleared and CE-marked smart ultrasound software for breast cancer risk assessment; FDA K212616 materials describe Koios DS as an AI/ML CADx adjunct for diagnostic ultrasound examinations of suspicious breast lesions and thyroid nodules.

Not for: Screening mammography replacement, standalone breast cancer diagnosis, unsupported patient groups, or use outside the cleared ultrasound indication.

What to verify before using Koios DS Breast

Source links

Use these links to confirm current claims, terms, regulatory status, pricing, and deployment requirements.

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