# Flinn

> Flinn (flinn.ai) is an AI-powered regulatory and quality platform for medical technology and in-vitro diagnostics (IVD) manufacturers. It automates post-market surveillance (PMS) and compliance across the EU MDR, IVDR, and FDA 21 CFR frameworks — monitoring 15+ safety databases, running AI-assisted literature evaluation, automating complaint handling, and producing audit-ready reports. Used by 200+ global MedTech and IVD organizations. Backed by HV Capital and Speedinvest.

Generated by the API Evangelist enrichment pipeline (method: generated) from apis.yml on 2026-07-19. Flinn is a closed SaaS application with no public developer API at this time.

## Company
- [Website](https://www.flinn.ai): Flinn AI regulatory and quality platform for MedTech/IVD.
- [About](https://www.flinn.ai/about): Company overview.
- [Blog](https://www.flinn.ai/blog): Regulatory and product updates.
- [Careers](https://career.flinn.ai/): Open roles.
- [Press](https://www.flinn.ai/press): Press and media.
- [Contact / Book a Demo](https://www.flinn.ai/contact): Sales and demo requests.
- [Login](https://app.flinncomply.com/login): Customer application sign-in.

## Security & Compliance
- [Security & Compliance](https://www.flinn.ai/security): ISO/IEC 27001:2022, ISO/TR 80002-2, IEC 62304, ISO 14971, FDA 21 CFR Part 11, EU AI Act, GDPR. AWS Frankfurt (eu-central-1) EU-only hosting; AES-256 encryption; no customer data used for model training.
- [Privacy Policy](https://www.flinn.ai/privacy): Data protection and privacy.
- [Legal Notice](https://www.flinn.ai/legal): Imprint and legal terms.

## Product
- Post-market surveillance (PMS) automation for low- to high-risk medical devices.
- Continuous monitoring of 15+ safety databases in a single click.
- AI-assisted literature evaluation and de-duplication.
- Complaint handling automation and audit-ready report generation.