Legal Framework
Terms of Service
Last Updated: May 13, 2026
Service Overview
Clearance AI provides AI-driven regulatory intelligence tools to assist in medical device classification and predicate search. While we strive for 100% accuracy through grounded reasoning, our platform is intended to assist professionals and does not constitute legal or regulatory advice.
Regulatory Disclaimer
Important
The final responsibility for all FDA submissions rests with the device manufacturer. Clearance AI's output should be verified by a qualified regulatory professional before submission.
User Responsibilities
Users are responsible for the accuracy of the information provided to the platform. Misrepresentation of device specifications may result in incorrect classification strategy.