Security
Layered security for every product lifecycle stage
From device development to fleet and operational management, ensure embedded security, verification, and control at each step.
Achieve compliance, stay competitive
The EU Cyber Resilience Act is here. Are you ready?
Complying with the EU Cyber Resilience Act (CRA) isn’t one-size-fits-all. Class I and II products — from smart home devices to essential enterprise tools — face unique standards to ensure safety and security. Read our complete guide on complying with the European Union Cyber Resiliency Act, and how over-the-air (OTA) updates are foundational to ensuring device security.
Ensure IoT device security across environments, complexity, and scale
Security by design
Trust a secure infrastructure
From initial design to product release, internal processes to external auditing, trust an OTA update solution with security embedded at every step.
Product security
Protect each device
Ensure security throughout the product lifecycle with secure first boot update, device authentication, code signing verification, mutual TLS (mTLS), and remote configuration.
Fleet security
Manage security at scale
Automatic retry, phased deployments, automated rollback, and full image updates protect IoT device fleets – regardless of scale, geographic location, or complexity.
Operational security
Secure internal processes
Multi-factor authentication, role-based access control (RBAC), audit logs, and single sign-on (SSO) reinforce security strategies throughout operations and the device lifecycle.
Security compliance
Meet regulations & standards
EU Cyber Resilience Act, ISA/IEC 62443, ISO/IEC 27001, ISO 26262, and more; out-of-the-box and automated features enable you to seamlessly prove compliance and meet security requirements.
Customer story
Case study: KVH
Navigating FDA and MDR Compliance: Managing the Device Lifecycle and Embedded Software Updates in Medical Devices - Dr. Baya Oussena
Regulatory bodies, such as the U.S. Food and Drug Administration (FDA) and the Medical Device Regulation (MDR), ensure the safety, effectiveness, and quality of medical devices. For software-driven devices, compliance is an ongoing process; each update or modification can present regulatory challenges for manufacturers. The rapid pace of software innovation makes navigating regulations more complex. Proactively addressing these challenges enhances quality, improves reliability and safety, and adds value for both patients and healthcare providers.
Preparing for the U.S Food and Drug Administration (FDA) premarket and 510(k) submissions
Expanded health access with telemedicine and digital health solutions; personalized healthcare and advanced detection and monitoring for improved patient outcomes. Operational efficiencies through automation, digitalization, and entirely new workflows. Promising cutting-edge Internet of Medical Things (IoMT) and AI-powered solutions tackling today's most challenging issues. For the medical and healthcare industry, technology holds massive untapped potential. Yet, it also comes with novel challenges.
Securing healthcare, medical, and Internet of Medical Things (IoMT) devices
The rapid growth of IoMT and escalating cybersecurity threats make it necessary for healthcare and medical OEMs to adopt a medical-grade OTA update strategy. Solutions must both address immediate security concerns while simultaneously accommodating regulations like FDA 501(k) and the NIS2 directive.