Cataract Surgeons Gain a New Lens Tool
An extended depth of focus intraocular lens approved by the FDA is designed to improve visual range while maintaining contrast sensitivity in cataract surgery.
The FDA has approved the TECNIS PureSee intraocular lens (IOL) for cataract surgery, a device designed to combat vision loss associated with cataracts and presbyopia. As patients age, cataracts can impair essential activities such as reading and driving. This extended depth of focus IOL aims to facilitate improved distance and intermediate vision, while offering some near vision capabilities. Notably, it is the first approved IOL in the US without warnings concerning loss of contrast sensitivity, proving effective in clinical evaluations. The lens is slated for US availability in 2026.
1. TECNIS PureSee IOL approved by FDA. 2. Designed for cataract surgery and addresses presbyopia. 3. Offers improved intermediate vision with some near capability. 4. Maintains contrast sensitivity like aspheric monofocal IOLs. 5. 97% of patients reported no major vision disturbances. 6. 2026 US market availability planned. 7. Includes a toric version for patients with astigmatism. 8. Used in nearly half a million eyes globally.