Postmarket· Jun 13, 2026
CISA KEV Catalog: Prioritize Device Risk
The CISA KEV catalog explained: who must act on it, how it drives SBOM and VEX triage, and how it fits postmarket obligations under the FDA's guidance.
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Looking for a quick answer instead? The FDA medical device cybersecurity FAQ covers Section 524B scope, SBOMs, threat models, CR515 and GMLP, deficiencies, and postmarket duties.
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