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Classify Your Medical Device | FDA

    https://www.fda.gov/medical-devices/overview-device-regulation/classify-your-medical-device
    The three classes and the requirements which apply to them are: Device Class and Regulatory Controls 1. Class I General Controls With Exemptions Without Exemptions 2. Class II General Controls...

Overview of Medical Device Classification and …

    https://www.fda.gov/about-fda/cdrh-transparency/overview-medical-device-classification-and-reclassification
    The FDA categorizes medical devices into one of three classes – Class I, II, or III – based on their risks and the regulatory controls necessary to provide a reasonable assurance of …

Device Classification Panels | FDA

    https://www.fda.gov/medical-devices/classify-your-medical-device/device-classification-panels
    FDA has classified and described over 1,700 distinct types of devices and …

Product Code Classification Database | FDA

    https://www.fda.gov/medical-devices/classify-your-medical-device/product-code-classification-database
    The Product Classification Database contains medical device names and associated information developed by the Center for Devices and Radiological Health (CDRH) in …



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