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The Ophthalmologist / Issues / 2026 / March / FDA Approves TECNIS PureSee IOL for Cataract Surgery
Cataract Refractive News

FDA Approves TECNIS PureSee IOL for Cataract Surgery

First FDA-approved extended depth of focus (EDOF) IOL maintaining contrast sensitivity comparable to an aspheric monofocal IOL

3/23/2026 2 min read

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5 Key Takeaways
  • 1

    The FDA has approved the TECNIS PureSee IOL, an extended depth of focus intraocular lens for cataract surgery.

  • 2

    TECNIS PureSee IOL will be available to US patients later this year, enhancing vision restoration opportunities.

  • 3

    This IOL addresses cataract-related vision loss and presbyopia in a single surgical procedure.

  • 4

    It is the first FDA-approved EDOF IOL with no warning on loss of contrast sensitivity, maintaining visual clarity.

  • 5

    97% of patients report minimal visual disturbances post-surgery, reducing their reliance on glasses.

This content is an AI-generated, fully rewritten summary based on a published scholarly article. It does not reproduce the original text and is not a substitute for the original publication. Readers are encouraged to consult the source for full context, data, and methodology.

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