The Medical Device Industry Database
Your Gateway to the Medical Device Industry
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Notified Bodies
Find 53 EU Notified Bodies designated for MDR and IVDR conformity assessment.
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Access 175 MDCG guidance documents and regulatory resources.
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Search 5,064 FDA-cleared medical devices with 510(k) and PMA data.
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Browse 3,311 FDA-registered manufacturers, distributors, and service providers.
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All DocsPresenting Risk Information in Prescription Drug and Medical…
FDA Guidance · 2009-05-01Human Factors Studies and Related Clinical Study Considerations…
FDA Guidance · 2016-02-01Modifications to Devices Subject to Premarket Approval (PMA)…
FDA Guidance · 2008-12-01Guidance for the Use of Bayesian Statistics in…
FDA Guidance · 2010-02-01Latest News
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Conferences
RSNA 2026 Annual Meeting to Advance Radiology and Medical Imaging Technology
February 18, 2026
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MedTech World Malta 2026 to Bridge Global MedTech Communities at the Mediterranean Crossroads
February 18, 2026
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MEDICA 2026 to Showcase 5,000+ Medical Technology Exhibitors From 70+ Nations
February 18, 2026
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