Robotic algorithm design that passes FDA/TÜV
Robotic algorithm design
We build safety-critical motion control, perception, and path-planning systems for industrial, medical, and autonomous mobile robots - designed from day one to pass ISO 13482, ISO 10218, IEC 61508, and FDA/CE audits on the first submission.
Selected client outcomes
- Full source code (C++ / Python / ROS 2) + detailed documentation
- 100% IP ownership transferred to you - no royalties. Ever.
- 12-month warranty: unlimited bug fixes & minor enhancements
- 42% faster time-to-market (based on 14 client projects, 2023-2025)
Zero commitment. In 30 minutes, we’ll show you how to cut 6-12 months off your roadmap.
Trusted by engineering teams at leading robotics companies in:
Traditional engineering firms
- $300k+engagements with vague deliverables
- 18-24 month timelines
- Limited hands-on robotics expertise
Clearpath Robotics Engineering (formerly The House of Design Robotics)
- Production-ready algorithms in ≤20 weeks
- 100% IP ownership - signed at project close
- First-time pass on FDA 510(k), TÜV, and CE audits
- Fixed-price contracts with agile collaboration
- Co-development: your engineers review code every sprint
What we deliver
You own everything - With full compliance
- Complete source code + architecture documentation
- Perpetual, royalty-free commercial license
- 100% IP ownership transferred upon final payment
- 12-month warranty - unlimited support for bugs and minor tweaks
- Mutual NDA + GDPR & ISO 27001-aligned development
- Agile co-development: Git, bi-weekly demos, CI/CD pipelines
Frequently Asked Questions
Do you deliver hardware or only software?
We specialize in production-grade software, but can recommend or integrate with hardware (NVIDIA Jetson, STM32, etc.). You keep full control of your stack.
Who owns the IP?
You do — 100%. All code, models, and documentation become your property upon final payment. We sign mutual NDAs before any technical discussion.
Are your systems actually certified?
Yes. Every safety-critical module is built to comply with ISO 13482 (personal care robots), ISO 10218 (industrial robots), IEC 61508 (functional safety), and FDA guidance. Clients have achieved CE, TÜV, and FDA clearance on first submission.
How long does a typical project take?
Full production systems: 12–20 weeks. Proof-of-concept or MVP: 4–8 weeks. Fixed timelines, fixed price.
Ready to De-Risk your certification & accelerate launch?
Book a free 30-minute technical consultation. We’ll audit your current stack and give you a custom roadmap to save 6-12 months.