Medical Device Databases

Please remove non-alphanumeric characters from your search terms.

For information on CDRH Databases, please visit:

http://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/Databases/default.htm

Other Databases

• 510(k)s
• De Novo
• Medical Device Reports (MAUDE)
• CDRH Export Certificate Validation (CECV)
• CDRH FOIA Electronic Reading Room
• CFR Title 21
• CLIA
• Device Classification
• FDA Guidance Documents
• Humanitarian Device Exemption
• Medsun Reports
• Premarket Approvals (PMAs)
• Post-Approval Studies
• Postmarket Surveillance Studies
• Radiation-Emitting Products
• Radiation-Emitting Electronic Products Corrective Actions
• Recalls
• Registration & Listing
• Standards
• Total Product Life Cycle
• X-Ray Assembler