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How Are Medical Devices Classified in the United States?
Category：企業(yè)動態(tài) Date：2024-11-20 17:05:05 Author: Source:
This classification system helps determine the level of regulatory scrutiny each device undergoes before it can be marketed in the United States.

In the United States, medical devices are classified into three main categories based on the level of risk they present to patients and the regulatory requirements needed to ensure their safety and effectiveness. The FDA (Food and Drug Administration) oversees the classification process, and the three classes are as follows:

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  1. Class I (Low Risk):

    • Definition: These are devices that present the lowest risk to patients.
    • Regulatory Requirements: Class I devices are subject to the least regulatory control. Most Class I devices are exempt from the premarket notification process (510(k)) and do not require Premarket Approval (PMA).
    • Examples: Bandages, manual surgical instruments, dental floss, and other basic devices.

  2. Class II (Moderate Risk):

    • Definition: Devices that carry a moderate risk to patients and require more regulatory oversight than Class I devices.
    • Regulatory Requirements: Class II devices generally require 510(k) clearance, meaning manufacturers must demonstrate that the device is substantially equivalent to an already legally marketed device.
    • Examples: Infusion pumps, surgical drapes, powered wheelchairs, and pregnancy test kits.

  3. Class III (High Risk):

    • Definition: These devices are considered the highest risk to patients and are typically used in situations where they sustain or support life, prevent impairment of health, or present potential for a significant risk of injury or illness.
    • Regulatory Requirements: Class III devices require Premarket Approval (PMA), which is a more stringent process that typically involves clinical trials to establish safety and efficacy.
    • Examples: Pacemakers, heart valves, deep brain stimulators, and certain types of implants.

Summary:

  • Class I: Low risk, minimal regulation.
  • Class II: Moderate risk, requires 510(k) clearance.
  • Class III: High risk, requires Premarket Approval (PMA).

This classification system helps determine the level of regulatory scrutiny each device undergoes before it can be marketed in the United States.

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