Now at SIIM 2026 · Startup Kiosk 3 · June 10–12

Trust

Compliance

On-premise architecture. Two FDA 510(k)-cleared products. No outbound PHI.

Security posture

The short version

On-premise, by default

Every product installs inside your institution's network. No cloud component carries PHI.

No outbound PHI

No telemetry, no auto-update over the internet, no patient data ever crosses the firewall.

Audit-ready

Every transformation is logged. Re-identification linking files stay on your storage.

Aligned with HIPAA

Because PHI processing happens on infrastructure you control, your institution's existing HIPAA controls apply directly.

FDA / 510(k) status

Two cleared products. The rest is research-use or in-development

  • INTContour510(k) K212274 · cleared 2022
    AI-assisted auto-contouring for radiation oncology.
  • INTDose510(k) K213137 · cleared 2022
    Monte Carlo dose verification for radiation treatment planning.
  • OncoAI Suite, QuantBrainNot FDA-cleared. Research-use only. Outputs are not for diagnostic or clinical decision-making purposes.
  • CuratAINot a medical device. Research-use data-curation platform. Not a diagnostic, treatment-planning, or clinical decision-support tool.

For product-specific deployment architecture, data-handling details, BAAs, DICOM Conformance Statements, or InfoSec questionnaire responses, contact [email protected]. See each product page for its own on-premise specifics.

Need a deeper security review?

We will walk your IT and compliance teams through architecture, controls, and audit logs.