Hardware compliance
without the guesswork.

Fuchsia is a hardware compliance platform that gets products certified faster. It maps your product to the standards that apply to it, drafts the technical documentation your testing lab needs, and matches you with a qualified lab - covering FCC, CE, UL, FDA 510(k), and ISO certifications. Fuchsia removes compliance as the bottleneck that stalls procurement and deployment.

Fuchsia replaces the slow, expensive consultant model with software that works on your timeline. A consultant charges by the hour and becomes a single point of delay; Fuchsia's research agent surfaces every applicable requirement with citations, then drafts lab-ready documentation in a fraction of the time. You keep the work in-house and move straight to testing instead of waiting on a third party.

Fuchsia does not run the lab tests itself; it gets you ready for them and matches you with the right lab. Fuchsia maps your requirements, drafts the documentation labs require, and then connects you with testing partners that specialize in your product category. This means you arrive at the lab with complete paperwork and skip the back-and-forth that usually delays testing.

Fuchsia works with hardware teams building IoT devices, robotics, medical devices, and aerospace and defense hardware. Any company that needs to clear FCC, CE, UL, FDA 510(k), or ISO standards before selling or deploying a physical product is a fit. Fuchsia is built for teams that treat compliance as a step on the path to shipping, not their core expertise.

Most electronic products sold in the United States need FCC authorization for their radio and electromagnetic emissions, and many also require UL safety certification to satisfy retailers and buyers. Medical devices additionally need FDA clearance, typically a 510(k). The exact set depends on your product category, which is what Fuchsia's research agent maps for you.

FCC certification authorizes a product for sale in the United States, while CE marking grants access to the European market. FCC focuses on radio frequency and electromagnetic emissions; CE marking is a broader self-declaration covering safety, EMC, and other EU directives that apply to your product. A product sold in both regions generally needs both.

Many industrial and service robots need UL certification, often UL 3300 for service robots, before a buyer will authorize deployment on a factory floor. Buyers and facilities frequently require a completed hazard analysis (HARA) alongside the certification. Missing either is a common reason procurement gets put on hold, which is exactly the kind of blocker Fuchsia surfaces early.

A testing lab typically needs your product's technical specifications, block diagrams, a bill of materials, test plans tied to the applicable standards, and supporting safety or risk analysis. Incomplete documentation is the most common reason testing stalls. Fuchsia drafts this lab-ready package automatically once your requirements are mapped, so you reach the lab ready to test.

Hardware compliance testing costs vary widely by product category and the standards involved, commonly ranging from a few thousand dollars for a single FCC test to tens of thousands for a full multi-standard medical or aerospace program. But the larger hidden cost is time: weeks spent researching requirements and compiling lab paperwork before testing even begins, plus expensive re-test cycles after failed or incomplete submissions. Fuchsia attacks both - accelerating the documentation work upfront and mapping requirements correctly so you avoid the delays and re-tests that drive the real cost.

Fuchsia's research agent takes your product details and identifies every standard that applies, returning the specific requirements with citations your team can verify and defend. Instead of manually combing through FCC, CE, UL, FDA, and ISO frameworks, you get a structured, cited map of what clearance requires for your exact product. This becomes the foundation for the documentation Fuchsia drafts next.

You can get started by booking a short call with the Fuchsia team, after which the research agent can begin mapping your product's requirements. Because Fuchsia is software rather than a consulting engagement, there is no long onboarding - you move from requirement mapping to lab-ready documentation quickly. Book a call to scope your specific product.

Fuchsia compresses the slowest part of compliance - researching requirements and drafting documentation - from months of manual work into a couple weeks, hands-off. Doing it yourself means combing through FCC, CE, UL, FDA, and ISO frameworks by hand and assembling lab paperwork from scratch, which is where most timelines slip. Fuchsia uses agents to automate this process, drastically accelerating shipping. Fuchsia does not change how long a lab takes to test, but it gets you to the lab ready, sooner.

Yes. Fuchsia is built to map several products and several standards in parallel, which is common for hardware companies shipping a product line or selling into multiple regions. Each product gets its own requirement map and documentation set, while you track everything together. This is a fit for teams certifying a portfolio rather than a single device.

Fuchsia helps you reduce failed tests in the first place and supports the documentation work if a re-submission is needed. Most test failures trace back to incomplete or incorrect documentation and missed requirements, which is exactly what Fuchsia's requirement mapping is designed to catch upfront. If a re-test is required, your requirement map and drafts are already in place to update and resubmit quickly.

Fuchsia works alongside your existing team and makes it faster, rather than replacing it. Regulatory staff use Fuchsia to skip manual requirement research and first-draft documentation, then focus their expertise on review and strategy. Teams without dedicated compliance staff use Fuchsia to cover work they would otherwise outsource to a consultant. Either way, the cited requirements keep your team in control of what gets submitted.