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CVE-2026-49009 & CVE-2026-33552 - Input sanitization and access control issues in Mender Server
Two security vulnerabilities recently discovered and fixed in Mender Server.
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3 min read
CVE-2025-67903 - Signature verification bypass in Mender Client
Security vulnerability enabling signature verification bypass in Mender Client version 5.0.0 to 5.0.3.
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2 min read
Official release: Mender for Microcontrollers (MCUs), like Zephyr, and the Micro Device Tier
Mender launches support for microcontrollers with the new Micro Device Tier, enabling efficient OTA updates for resource-constrained devices like Zephyr-based MCUs.
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10 min read
Success with AI in MedTech depends on the software infrastructure beneath it
Explore how robust software infrastructure is essential for the success of AI in MedTech, ensuring compliance, security, and lifecycle sustainability in medical devices.
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3 min read
Succeeding in the IoT product landscape: How OEMs align AI, software, and time-to-Market
Discover how OEMs can effectively align AI and software to enhance their IoT products, tackle time-to-market challenges, and ensure long-term success.
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4 min read
What’s new in Mender: New Update Modules for container updates
Discover Mender's new Update Modules for OTA container updates, enhancing deployment efficiency and network reliability for seamless software updates.
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3 min read
Insights from Embedded World 2026: The looming EU CRA deadlines driving imminent change
Explore the impact of the EU Cyber Resilience Act on OEMs at Embedded World 2026, highlighting compliance challenges and the need for robust OTA update strategies.
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4 min read
Beyond traditional connectivity: managing smart products and machines in air-gapped and offline environments
Explore how to manage smart devices in air-gapped and offline environments with secure, authenticated software updates, ensuring compliance and operational efficiency.
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7 min read
Key considerations: How to build compliant software update practices for medical devices
Learn how to implement compliant software update practices for medical devices while navigating FDA and EU MDR regulations, ensuring safety and cybersecurity.
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7 min read







