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Medical Devices
FDA's Role in Fostering the Development of Better Medical Devices
Message from Center Director Jeff Shuren, M.D., J.D.
Products and Medical Procedures
Approvals & Clearances, Home Use, Surgical, Implants & Prosthetics, In Vitro Diagnostics, more...
Medical Device SafetyAlerts & Notices, Recalls, Report a Problem, MedSun, Emergency Situations
Device Advice: Device Regulation and GuidanceHow to Market a Device, Postmarket Requirements, Compliance, Importing & Exporting, more...
Science and Research (Medical Devices)
Chemistry & Materials Science, Solid & Fluid Mechanics, Imaging & Applied Mathematics, Electrical & Software Engineering, more...
News & Events (Medical Devices)Medical Device News, Videos, Workshops & Meetings
Resources for You (Medical Devices)Consumers, Health Care Providers, Regulated Industry
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Program Areas
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Industry Assistance
CDRH Learn Guidance Documents (Medical Devices and Radiation-Emitting Products) How to Market Your Device Postmarket Requirements (Devices) Importing and Exporting Devices International Information (Devices) Device Classification Bioresearch Monitoring FDA eSubmitter Resolution of Differences of Opinion
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Spotlight
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Recalls & Alerts
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Approvals & Clearances
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Tools & Resources
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Contact Us
CDRH-Center for Devices and Radiological Health
- 1-800-638-2041
- 301-796-7100
Food and Drug Administration
10903 New Hampshire Avenue
WO66-5429
Silver Spring, MD 20993
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