THE NEW TECNIS® 1-PIECE IOL PROVIDES THE UNMATCHED BENEFITS OF TECNIS® TECHNOLOGY IN A NEXT-GENERATION ONE-PIECE DESIGN

OPTICS:
The first and only FDA-approved wavefront-designed optic that rejuvenates vision by correcting spherical aberration to essentially zero.

MATERIAL:
The proprietary hydrophobic acrylic material with the lowest chromatic aberration and highest optical throughput transmits healthy blue light and reduces the incidence of glistenings.

DESIGN:
The only one-piece lens with the performance of a ProTEC™ 360° barrier edge, the stability of Tri-Fix™ 3-point design, and a frosted edge treatment.

ADVANCED TECHNOLOGIES THAT CREATE OPTICAL SYNERGY

This proprietary combination of optic, material, and design technologies work together to create Optical Synergy for superior visual results.

Indications and Important Safety Information

TECNIS® IOLs

Caution

Federal law restricts this device to sale by or on the order of a physician.

Indications

Tecnis® lenses are indicated for the visual correction of aphakia in adult patients in whom a cataractous lens has been removed by extracapsular cataract extraction. These devices are intended to be placed in the capsular bag.

Warnings

Physicians considering lens implantation under any of the conditions described in the Directions for Use labeling should weigh the potential risk/benefit ratio prior to implanting a lens.

Precautions

Do not resterilize or autoclave. Use only sterile irrigating solutions such as balanced salt solution or sterile normal saline. Do not store in direct sunlight or over 45°C.

Adverse Events

Adverse events occurred at rates between 1.6% and 3.3% during the clinical trials for Tecnis® IOLs or their “parent” IOLs. These events included macular edema, endophthalmitis, anterior lens tissue ongrowth, lens dislocation, hypopyon, corneal edema, iritis, hyphema, secondary glaucoma, and secondary surgical intervention. 

Attention

Reference the Directions for Use for a complete listing of indications, warnings, and precautions.

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