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CATEGORY: REGULATORY PATHWAYS

Breakthrough Device Designation

An FDA program providing prioritized review for devices that offer more effective treatment or diagnosis of life-threatening or irreversibly debilitating conditions. Provides interactive review, priority review, and senior management involvement.

Last reviewed 2026-08-05 · Reviewed by MedFlux Editorial Board · Editorial policy

WHEN IT APPLIES

FDA Breakthrough Device Designation prioritizes devices for more effective treatment/diagnosis of life-threatening or irreversibly debilitating conditions.

PROCESS / STEPS

  1. Assess eligibility against FDA breakthrough criteria.
  2. Request designation with preliminary data package.
  3. Use interactive review features during premarket submission.
  4. Maintain postmarket commitments if applicable.

EXAMPLES

  • Novel diagnostics addressing serious unmet needs often pursue breakthrough designation.

RELATED GUIDES & TOOLS

SOURCES

Track regulatory signals related to Breakthrough Device Designation across 27 authorities in real time.

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