SBOM Management in 2026
Software Bills of Materials for medical devices: generation, monitoring, and using SBOMs as a continuous security tool, not a checkbox.
SBOMs are now mandatory for FDA cybersecurity submissions, but most teams still treat them as a one-time deliverable. These episodes show how to generate accurate SBOMs, monitor them for new vulnerabilities, link them to your threat model, and use them throughout the device lifecycle. Tooling (CycloneDX, SPDX), automation, and integration with your secure SDLC are all covered.
This page rounds up every SBOM Management conversation we've published in 2026 on The Med Device Cyber Podcast. Each episode pairs an experienced practitioner - a regulator, a startup founder, a security researcher, or a quality lead - with our hosts, who've personally led FDA premarket and postmarket cybersecurity submissions for connected medical devices. The result is a working library of frameworks, war stories, and reviewer-tested patterns you can apply to your own 510(k), De Novo, or PMA program.
Use the 2026 archive below to get a sense of how sbom expectations are evolving this year - what the FDA is asking for in deficiency letters, which engineering practices the field is converging on, and where reasonable people still disagree. If you want a longer-running view, browse the full SBOM Management topic page for every episode we've ever published on the subject, or jump to the complete 2026 catalog to see what else aired alongside these episodes.
