Risk· Jun 5, 2026
MQTT Vulnerabilities in Connected
MQTT is one of the most common protocols in IoMT and one of the most commonly misconfigured.
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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.
Showing 12 of 23 articles in Risk · Page 1 of 2
MQTT is one of the most common protocols in IoMT and one of the most commonly misconfigured.
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Where CAN/CANopen shows up inside medical devices, the attack paths reviewers want modeled, and the controls that actually hold up under pen test.
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Discover the top 10 medical device cybersecurity vulnerabilities from real-world penetration testing & learn how to protect patients and meet FDA.
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The PATCH Act became section 524B and covers new cyber devices only. See what it requires, who is exempt, and how to secure legacy medical devices.
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Explore the critical distinctions between safety and security risks in medical devices. Aligned with the FDA's Feb 3, 2026 premarket cybersecurity guidance.
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Explore QNX operating system vulnerabilities, risks, and mitigation strategies crucial for medical devices. Understand how to secure QNX-based systems.
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Medical Device Cybersecurity Risk Profiles for medical devices: step-by-step practices, FDA-aligned documentation, and pitfalls to avoid in 2026 submissions.
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Cellular connectivity medical device security: 2G/3G downgrade risk, IMSI catchers, eSIM provisioning, LTE/5G, modem data at rest, and FDA documentation.
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The risks and vulnerabilities in M2M communication between connected medical devices, and the cybersecurity controls the FDA expects at premarket review.
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Medical device interoperability creates shared risk across vendors. Learn where trust breaks down, what the FDA expects in labeling, and how to document it.
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Explore the potential vulnerabilities in MedRadio and delve into the crucial aspects of medical device cybersecurity in this insightful article.
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QIH Medical Device Vulnerabilities in medical devices: attack scenarios, patient-safety impact, and mitigations FDA reviewers expect in 2026 submissions.
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