Contributors

Meet the experts and professionals who build and maintain Medical Device Navigator — the world's most comprehensive free medical device intelligence platform.

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Founder & Lead Contributor

HR

Dr. Hatem Rabeh

MD, MSc Ing — Clinical Evaluation Expert & Regulatory Affairs Specialist

Dr. Hatem Rabeh is the founder of Medical Device Navigator and the architect of its regulatory intelligence database. With a background in medicine (MD) and engineering (MSc Ing) from Université Grenoble Alpes, he brings deep expertise in clinical evaluation, EU MDR/IVDR compliance, and FDA regulatory pathways. Medical Device Navigator was created to democratise access to medical device regulatory information — providing free, comprehensive, and up-to-date data for industry professionals worldwide.

Clinical Evaluation EU MDR / IVDR FDA Regulatory 510(k) & PMA Regulatory Affairs Université Grenoble Alpes

Platform at a Glance

4,975 FDA-registered Companies
5,064 Cleared Devices
1,129 Resources & Guidelines

How to Contribute

  • Submit a Data Correction

    Spotted an error in a device listing, company profile, or regulatory document? Send us a correction request and we'll review it within 48 hours.

  • Submit a Press Release

    Share your company's regulatory milestones, product clearances, or industry news with thousands of medical device professionals.

  • Expert Article Contribution

    Regulatory affairs experts, clinical evaluation specialists, and industry veterans are welcome to contribute technical articles and analysis.

  • Report a Missing Entry

    Know of a company, device, notified body, or regulatory guidance that's not in our database? Let us know and we'll add it to our queue.

Contact the Team

Response 1–2 business days
Coverage FDA · EU MDR/IVDR · MHRA · Swissmedic · Health Canada
Founded 2024

Contribute to MDN

Have expertise to share or data to submit? We welcome contributions from regulatory professionals worldwide.

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