Health ISAC Spring Summit 2026

As medical devices become more connected and software-driven, manufacturers face growing pressure to manage risk, meet regulatory requirements, and prove security across the entire device lifecycle, where gaps can directly impact patient safety.

From FDA 524B premarket requirements to postmarket obligations and SBOM mandates, Finite State replaces fragmented tools and manual processes with a continuous, evidence-backed system that supports regulatory readiness while helping teams identify and address risks before they impact devices in the field.

🔎 Visit Our Booth to See:

Live demos of artifact-backed workflows built for medical devices

• Firmware-grounded inventory and SBOM management
  Create a complete, versioned system of record across firmware, binaries, source, and supplier SBOMs to support FDA and global regulatory requirements
• Exposure-driven prioritization
  Use reachability and device context to reduce vulnerability noise and focus remediation on what is truly relevant to patient safety
• New CVE to impacted devices
  Quickly determine which builds, variants, and fielded products are affected and generate consistent, defensible VEX decisions
• Submission-ready evidence, continuously maintained
  Produce SBOM, VEX, traceability, and verification evidence that stays current across development and postmarket updates
• Design-to-build traceability
  Maintain alignment between architecture, risks, requirements, and shipped software to support secure-by-design expectations

📅 Book a 1:1 Meeting

Plan your path to FDA 524B readiness and continuous medical device security

Meet with our team in Tampa to:

• Prepare premarket submissions with audit-ready SBOM, risk documentation, and evidence workflows
• Reduce vulnerability noise with reachability-based prioritization and defensible decisions
• Accelerate postmarket response from new CVE to impacted devices and customer-ready outputs
• Build a firmware-grounded system of record across products, variants, and suppliers
• Maintain compliance evidence continuously without rebuilding documentation for each submission

🛡️ Why Finite State for Medical Device Security?

• Built for connected and embedded medical devices, not just source code
• Unifies firmware, binary, and source intelligence into a single system of record
• Prioritizes real exposure with reachability and device context
• Maintains continuous SBOM, VEX, and evidence workflows across the device lifecycle
• Produces submission-ready and audit-ready outputs for FDA and global regulations
• Supports both security and compliance teams in one platform

🎁 Bonus: Insights + Resources

Stop by our booth for expert guidance on medical device security, regulatory readiness, and practical workflows you can apply immediately.

Protect patient safety. Prove compliance continuously. Automate the work in between.

Health ISAC Spring Summit 2026 | Tampa, Florida
We hope to see you there.