Skip to main content

EXPLORE

TECNIS SYMFONY® Extended Depth of Focus IOL

Mitigate the effects of presbyopia while delivering brilliant, continuous vision.

TECNIS SYMFONY® Toric Extended Depth of Focus IOL

Address both presbyopia and astigmatism while delivering continuous vision. 

DISCOVER

ifs

Surgical Systems

Find out more about our platforms for LASIK and cataract surgery.

Customer Support

CUSTOMER SUPPORT

Explore resources for equipment education and practice development, as well as our online tools.

INDICATIONS AND IMPORTANT SAFETY INFORMATION FOR TECNIS SYMFONY® AND TECNIS SYMFONY® TORIC EXTENDED RANGE OF VISION IOLs

Rx Only

INDICATIONS

The TECNIS Symfony® Extended Range of Vision IOL, model ZXR00, is indicated for primary implantation for the visual correction of aphakia, in adult patients with less than 1 diopter of pre-existing corneal astigmatism, in whom a cataractous lens has been removed. The lens mitigates the effects of presbyopia by providing an extended depth of focus. Compared to an aspheric monofocal IOL, the lens provides improved intermediate and near visual acuity, while maintaining comparable distance visual acuity. The model ZXR00 IOL is intended for capsular bag placement only. The TECNIS Symfony® Toric Extended Range of Vision IOLs, models ZXT150, ZXT225, ZXT300, and ZXT375, are indicated for primary implantation for the visual correction of aphakia and for reduction of residual refractive astigmatism in adult patients with greater than or equal to 1 diopter of preoperative corneal astigmatism, in whom a cataractous lens has been removed. The lens mitigates the effects of presbyopia by providing an extended depth of focus. Compared to an aspheric monofocal IOL, the lens provides improved intermediate and near visual acuity, while maintaining comparable distance visual acuity. The model series ZXT IOLs are intended for capsular bag placement only.

WARNINGS

Physicians considering lens implantation under any of the circumstances described in the Directions for Use should weigh the potential risk/benefit ratio as such patients may not be suitable candidates for an intraocular lens because the lens may exacerbate an existing condition, may interfere with diagnosis or treatment of a condition, or may pose an unreasonable risk to the patient’s eyesight.

ATTENTION

Reference the Directions for Use for a complete listing of Indications and Important Safety Information.

See Full Indications and Important Safety Information for the TECNIS Symfony® IOL.

See Full Indications and Important Safety Information for the TECNIS Symfony® Toric IOL.

PP2018MLT4018