Turn local security scans into FDA-submission-focused evidence.
SCS helps Medtech regulatory and software teams produce FDA-submission-focused SAST and SBOM reports from local or CI scans, without sending source code outside their environment.
Security evidence built from the workflow teams already use.
Built for medtech and regulated software teams that need practical developer feedback and credible evidence for medical device submissions and design records.
From scanner output to submission-focused evidence.
SCS turns raw scanner output, SBOM files, and CI/CD signals into structured outcomes your team can review, gate, and export for submission work.
Run scanner
Use the SCS CLI in a local workspace or pipeline to collect SAST and SBOM data.
Upload results
Attach project, branch, commit, token, and scan configuration context.
Review evidence
Triage findings, inspect SBOM readiness, and capture FDA guidance review decisions.
Export reports
Produce SAST and SBOM evidence packages for FDA submissions and internal design records.