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Overview and Key Features of AcrySof® IQ ReSTOR® Multifocal IOLs

Explore the tabs below to learn:

  • How this innovative technology works
  • Key design differences between the AcrySof® IQ ReSTOR® +2.5 D IOL and the AcrySof® IQ ReSTOR® +3.0 D IOL
  • How best to select an AcrySof® IQ ReSTOR® IOL for your patients based on their lifestyle needs and vision goals

AcrySof® IQ ReSTOR® IOLs can help reduce spectacle dependence for all kinds of activities.

AcrySof® IQ ReSTOR® IOL Specifications

Specifications +2.5 +3.0 +4.0
Model Number SV25T0 SN6AD1 SN6AD3
Add Power +2.5 +3.00 D +4.00 D
Add-power Spectacle Plane +2.00 D +2.5 D +3.20 D
Number of Diffractive Steps 7 9 12
Filtration UV and Blue Light Filtering
Optic Material Acrylate/Methacrylate Copolymer
Central Optic Zone Distance Intermediate
Optic Diameter 6.0 mm
Overall Length 13.0 mm
A-constant* 119.1 118.9
Index of Refraction 1.55
Haptic Angulation
Haptic Configuration STABLEFORCE® Haptics

Click the rows above to explore the AcrySof® IQ IOL platform benefits of AcrySof® IQ ReSTOR® IOLs.

AcrySof® IQ ReSTOR® IOL lens diagrams

*Provided as a guideline only.


   
View Important Product Information for
AcrySof® IQ ReSTOR® Family of IOLs+

ACRYSOF® IQ RESTOR® FAMILY OF MULTIFOCAL IOLS IMPORTANT PRODUCT INFORMATION

CAUTION: Federal (USA) law restricts this device to the sale by or on the order of a physician.

INDICATIONS: The AcrySof® IQ ReSTOR® Posterior Chamber Intraocular Multifocal IOLs include AcrySof® IQ ReSTOR® and AcrySof® ReSTOR® Toric are intended for primary implantation for the visual correction of aphakia secondary to removal of a cataractous lens in adult patients with and without presbyopia, who desire near, intermediate and distance vision with increased spectacle independence. In addition, the AcrySof IQ ReSTOR Toric IOL is intended to correct pre-existing astigmatism. The lenses are intended to be placed in the capsular bag.

WARNINGS / PRECAUTIONS: Careful preoperative evaluation and sound clinical judgment should be used by the surgeon to decide the risk/benefit ratio before implanting a lens in a patient with any of the conditions described in the Directions for Use labeling for each IOL. Physicians should target emmetropia, and ensure that IOL centration is achieved. Care should be taken to remove viscoelastic from the eye at the close of surgery.

The ReSTOR Toric IOL should not be implanted if the posterior capsule is ruptured, if the zonules are damaged, or if a primary posterior capsulotomy is planned. Rotation can reduce astigmatic correction; if necessary lens repositioning should occur as early as possible prior to lens encapsulation.

Some patients may experience visual disturbances and/or discomfort due to multifocality, especially under dim light conditions. A reduction in contrast sensitivity may occur in low light conditions. Visual symptoms may be significant enough that the patient will request explant of the multifocal IOL. Spectacle independence rates vary; some patients may need glasses when reading small print or looking at small objects.

Posterior capsule opacification (PCO), when present, may develop earlier into clinically significant PCO with multifocal IOLs. Prior to surgery, physicians should provide prospective patients with a copy of the Patient Information Brochure available from Alcon informing them of possible risks and benefits associated with the AcrySof® IQ ReSTOR® IOLs.

Do not resterilize; do not store over 45° C; use only sterile irrigating solutions such as BSS® or BSS PLUS® Sterile Intraocular Irrigating Solutions.

ATTENTION: Reference the Directions for Use labeling for each IOL for a complete listing of indications, warnings and precautions.

Click here to view the AcrySof® IQ ReSTOR® +2.5 D IOL Directions for Use (DFU).

Click here to view the AcrySof® IQ ReSTOR® +3.0 D IOL Directions for Use (DFU).

ACRYSOF® SINGLE-PIECE MONOFOCAL INTRAOCULAR LENSES IMPORTANT PRODUCT INFORMATION

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

INDICATIONS: AcrySof® single-piece monofocal intraocular lenses (IOLs) include the AcrySof® IQ Aspheric Natural IOL (Model SN60WF), AcrySof® UV-Absorbing Aspheric IOL (Model SA60WF), AcrySof® Natural IOL (Model SN60AT) and AcrySof® IOL (Model SA60AT). Each IOL is indicated for visual correction of aphakia in adult patients following cataract surgery. These IOLs are intended for replacement in the capsular bag.

WARNINGS/PRECAUTIONS: Careful preoperative evaluation and sound clinical judgment should be used by the surgeon to decide the risk/benefit ratio before implanting an IOL in a patient with any of the conditions described in the Directions for Use that accompany each IOL. Caution should be used prior to lens encapsulation to avoid lens decentration or dislocation. Viscoelastic should be removed from the eye at the close of surgery.

Studies have shown that color vision discrimination is not adversely affected in individuals with the AcrySof® Natural IOL (Model SN60AT) and normal color vision. The effect on vision of the AcrySof® Natural IOL in subjects with hereditary color vision defects and acquired color vision defects secondary to ocular disease (e.g. glaucoma, diabetic retinopathy, chronic uveitis, and other retinal or optic nerve diseases) has not been studied.

Do not resterilize. Do not store at temperatures over 45° C. Use only sterile irrigating solutions to rinse or soak IOLs.

ATTENTION: Refer to the Directions for Use labeling for each IOL for a complete list of indications, warnings and precautions.

Click here to view the AcrySof® IQ IOL Directions For Use (DFU).