Hardware Compliance Software That Works in Weeks

Hardware Compliance supports a broad range of standards relevant to hardware product certification, including FCC, CE Marking, FDA 510(k), UL Certification, ISO 9001/9100, ISO 26262, FAA, UL 3100, UL 3300, IEC 62368-1, MIL-STD, ASTM, ANSI, and RIA. The platform is designed to cover the full range of standards hardware teams encounter across robotics, electronics, medical devices, drones, automotive electronics, and aerospace products.

Traditional compliance consultants bill by the hour and take months to deliver research and documentation by hand. Hardware Compliance's AI agents read and reason across the same regulatory standards and generate product-specific compliance outputs in a fraction of the time. Where a consultant's throughput is limited by headcount, Hardware Compliance scales with compute. Expert review and sign-off by industry professionals is also built into the platform, so you get AI speed with human accountability.

Hardware Compliance is built for physical hardware products across multiple industries. The platform serves robotics startups, electronics and IoT companies, drone manufacturers, medical device developers, automotive electronics teams, and aerospace and defense hardware suppliers. If your product needs safety certification or market access clearance — whether for the US, EU, UK, or other jurisdictions — Hardware Compliance's compliance software is designed to handle it.

Hardware Compliance replaces months of compliance consulting with a workflow that takes weeks. The exact timeline depends on your product type, the standards required, and your target markets. Hardware Compliance's AI agents dramatically accelerate the research and documentation phases that typically consume most of the pre-testing timeline, so your team can reach the testing lab stage faster and with complete, lab-ready documentation.

Hardware Compliance supports FDA 510(k) compliance as part of its hardware compliance software platform. The AI agents identify every applicable FDA requirement for your device, generate the required technical documentation and test plans, and match you with accredited testing labs appropriate for medical device certification. Expert review and sign-off is included before any documentation is submitted, providing an additional layer of accountability for high-stakes regulatory submissions.