INTContour
FDA 510(k)-cleared (K212274) AI auto-contouring platform for organ-at-risk and target segmentation in radiation oncology, covering over 120 structures across CT, MRI, and PET/CT with automatic quality assurance.
Where it ranks
Current edition · updated Oct 20, 2026What it does
FDA 510(k)-cleared (K212274) AI auto-contouring platform for organ-at-risk and target segmentation in radiation oncology, covering over 120 structures across CT, MRI, and PET/CT with automatic quality assurance.
- Clinical research data curation
- Radiation oncology treatment planning and QA
- Brain ventricle volumetrics for hydrocephalus
- Category
- Healthcare data and research
- Built for
- Healthcare and life sciences
- Users
- Academic medical centers, Research groups, Hospitals, Medical-device companies
- Public API
- Not offered
- Deployment
- On-premises
Not yet disclosed: platforms, languages and support channels.
Pricing
Pricing isn't published
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Security and compliance
As reported by Carina AI. Ask for audit reports before you buy.
- FDA 510(k) - INTContourCompliant
- FDA 510(k) - INTDoseCompliant
- On-premise by default — every product installs inside the institution's network; no cloud component carries PHI
- No outbound PHI — no telemetry, no auto-update over the internet, no patient data crosses the firewall
- Audit-ready — every transformation is logged; re-identification linking files stay on customer storage
- Software delivered to local computers with no retained remote access unless requested
- Locally installed products collect no data without user acknowledgement or permissions
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