FDA Clears Avulux Migraine Lenses - Scorecard - MDSpire
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FDA Clears Avulux Migraine Lenses

  • September 15, 2026

  • 2 min

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Clinical Scorecard: FDA Clears Avulux Migraine Lenses

At a Glance

CategoryDetail
ConditionMigraine-associated light sensitivity
Key MechanismsPrecision light-filtering lenses designed to block specific wavelengths of light (480 nm and 590 nm) while allowing the rest of the visible spectrum to pass through.
Target PopulationPatients aged 12 years and older with episodic migraine
Care SettingEye care providers and optical practices

Key Highlights

  • FDA granted De Novo marketing authorization for Avulux lenses.
  • Lenses block light at 480 nm and 590 nm, targeting light sensitivity.
  • Up to 90% of migraine patients experience light sensitivity.
  • Lenses are available over-the-counter and can be prescribed.
  • More than 50,000 users have been dispensed the lenses.

Guideline-Based Recommendations

Diagnosis

  • Patients should be diagnosed with episodic migraine and clinically significant light sensitivity.

Management

  • Patients are advised to continue standard migraine treatments alongside the use of Avulux lenses.

Monitoring & Follow-up

  • Monitor the effectiveness of the lenses in reducing light sensitivity and migraine attacks.

Risks

  • Potential for light sensitivity to trigger migraine attacks remains.

Patient & Prescribing Data

Adolescents and adults with episodic migraine experiencing light sensitivity.

Lenses are intended to complement existing migraine treatments, not replace them.

Clinical Best Practices

  • Educate patients on the use of Avulux lenses in conjunction with prescribed migraine medications.
  • Assess the impact of light sensitivity on patients' migraine frequency and severity.

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