Protect PHI and prove it every release
Healthcare products run in complex, highly regulated ecosystems with cloud services, apps, and third-party integrations. DevArmor embeds cybersecurity risk modeling and threat analysis into design and release workflows, following FDA and MITRE threat modeling guidance.
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Automate Threat Modeling and Security Risk Assessment
DevArmor aligns with the FDA/MDIC Playbook for Threat Modeling Medical Devices, automating the identification of high-value dataflows and trust boundaries across software, firmware, and cloud components.
Every project runs a continuous “Four Questions” loop — defining assets, evaluating what can go wrong, recommending mitigations, and validating results. This means cybersecurity design reviews are no longer one-time documents — they become living, testable controls tied to your design history file (DHF) and risk management process
(ISO 14971 / AAMI TIR57).
Continuous HIPAA & FDA Compliance Evidence
DevArmor automates the creation of DFDs, trust boundaries, and mitigation mappings across your codebase and CI/CD pipelines — providing the same outputs auditors expect from manual design control documentation.
How it works
Fetch business context and design specs
automatically via safe, configurable integrations
Create threat model
and generate requirements
In less than 10 minutes
Enforce design controls and guardrails
automatically pushed to downstream tools
Top Outcomes for HealthTech Teams
- 3–5x more design reviews with existing security staff
- Threat models automatically mapped to HIPAA/HITRUST and AAMI TIR57 controls
- Per-release compliance evidence without manual rework




























