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We're here to help accelerate your regulatory processes
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Have questions about our AI-powered regulatory submission platform? Need help with your FDA 510(k) submission? Want to explore partnership opportunities? We're here to help.
Address
80 Pinewood Rd
Hartsdale, NY 10530
United States
Response Time
We typically respond within 24 hours
Monday through Friday, 9 AM - 5 PM EST
Our Mission
At Cruxi, our mission is to accelerate regulatory processes for the good of patients. Every day a life-saving medical device is delayed in reaching patients is a day too many.
We're building AI-powered tools that streamline FDA submissions, reduce time-to-market, and bring innovative medical devices to patients faster—ultimately saving lives and improving healthcare outcomes.
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How We Can Help
Whether you're just getting started or need expert guidance
General Questions
Learn more about our platform, features, and how AI-powered regulatory tools can help your medical device company.
Technical Support
Get help with using our platform, troubleshooting issues, or understanding specific features and workflows.
Business Partnerships
Explore partnership opportunities, enterprise solutions, or integration with your existing regulatory workflows.
510(k) Submission Help
Get guidance on your FDA 510(k) submission, understand requirements, or learn best practices for regulatory compliance.
Pricing & Plans
Learn about our pricing structure, available plans, and find the right solution for your company's needs.
Feedback & Suggestions
Share your feedback, suggest new features, or let us know how we can improve our platform to better serve you.
Ready to Get Started?
Start your FDA 510(k) submission today and experience the power of AI-powered regulatory workflows.
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