Complizen is the AI-powered FDA compliance platform built for medical device startups, manufacturers, and consultants who need to get to market faster. Instead of wasting time digging through scattered FDA databases and guidance documents, teams use Complizen to instantly retrieve and interpret regulatory requirements, map out a clear 510(k) submission roadmap, and save 12+ hours each week on research. Startups gain investor-ready submissions in weeks, consultants scale their client work with confidence, and medtech companies accelerate time to market while staying compliant as they grow. By combining AI-driven guidance with a deep regulatory data graph, Complizen transforms compliance from a roadblock into a competitive advantage.