AcrySof® IQ ReSTOR® +2.5 D IOL

Recommend AcrySof® IQ ReSTOR® +2.5 D IOL with ACTIVEFOCUSTM optical design for your patients with active lifestyles,* such as those who:

  • Participate in activities requiring more intermediate (53 cm/21 in) and distance (4 m/13 ft) vision*
  • Are not willing to compromise distance vision for a full range
  • Desire more opportunity for a range of vision versus monofocal
  • Might prefer an alternative to monovision
  • Desire increased spectacle independence

The ACTIVEFOCUSTM optical design is engineered to take your patients’ distance vision a step further while providing the balanced near and intermediate performance with the goal of reducing spectacle dependence for activities like1-3:

  • Driving and dashboard viewing
  • Playing or watching live sports
  • Attending theater or performance events
*Active-lifestyle patients participate in activities that require intermediate and distance vision such as golf, tennis, house cleaning
and driving.

ACTIVEFOCUSTM Optical Design


AcrySof® IQ ReSTOR® +2.5 D IOL defocus curve3

ACTIVEFOCUSTM optical design is engineered to deliver:

  • Excellent, sharp distance vision3
  • Superior near (40 cm) and intermediate (53 cm) vision by two lines versus AcrySof® IQ monofocal IOL3
The majority of patients with AcrySof® IQ perform IOL implants report using distance vision glasses none of the time
  • AcrySof® IQ ReSTOR® +2.5 D IOL (n=130)
    (1-month post op data)
  • AcrySof® IQ ReSTOR® +4.0 D IOL (n=114)
    (6-month post op data)
  • AcrySof® IQ ReSTOR® +3.0 D IOL (n=116)
    (6-month post op data)
Click the legend items to toggle on and off for comparison.
The majority of patients with AcrySof® IQ perform IOL implants report using distance vision glasses none of the time

AcrySof® IQ ReSTOR® +2.5 D IOL contrast sensitivity3

For sharp distance vision and more, ACTIVEFOCUSTM optical design delivers3:

  • Same quality contrast sensitivity as AcrySof® IQ Monofocal IOL
AcrySof® IQ ReSTOR® +2.5 D IOL contrast sensitivity

Simulated retinal images using a Badal optometer (3 mm pupil)5

AcrySof® IQ ReSTOR® +2.5 D IOL simulated images

Simulated headlight images in Alcon model eye6
(5 mm pupil measured on the optikos MTF system)

AcrySof® IQ ReSTOR® +2.5 D IOL simulated headlight comparison

Visual disturbances3

Only 3.3% of patients implanted with AcrySof® IQ ReSTOR® +2.5 D IOLs experienced severe glare.3
Patients implanted with AcrySof® IQ Monofocal IOLs experienced 3.8% severe glare.3

AcrySof® IQ ReSTOR® +2.5 D IOL visual disturbances

**The safety of the AcrySof® IQ ReSTOR® +2.5 D Multifocal IOL Model SV25T0 is based in part on the safety demonstrated by parent models MA60D3 and SA60D3. No unanticipated serious adverse device effects were observed in any subjects implanted with Model SV25T0. There were no reports of explants during this clinical study.

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

ACRYSOF® IQ RESTOR® FAMILY OF INTRAOCULAR LENSES 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 Lens (IOL) is 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. The lens is 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. 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.

Some patients may experience visual disturbances and/or discomfort due to multifocality, especially under dim light conditions. As with other multifocal IOLs, visual symptoms may be significant enough that the patient will request explant of the multifocal IOL. Spectacle independence rates vary with all multifocal IOLs; as such, some patients may need glasses when reading small print or looking at small objects.

Clinical studies with the AcrySof® ReSTOR® lens indicated that posterior capsule opacification (PCO), when present, developed earlier into clinically significant PCO. Prior to surgery, physicians should provide prospective patients with a copy of the Patient Information Brochure available from Alcon for this product informing them of possible risks and benefits associated with the AcrySof® IQ ReSTOR® IOLs.

Studies have shown that color vision discrimination is not adversely affected in individuals with the AcrySof® Natural IOL 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 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 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® IQ RESTOR® FAMILY OF INTRAOCULAR LENSES 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 Lens (IOL) is 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. The lens is 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. 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.

Some patients may experience visual disturbances and/or discomfort due to multifocality, especially under dim light conditions. As with other multifocal IOLs, visual symptoms may be significant enough that the patient will request explant of the multifocal IOL. Spectacle independence rates vary with all multifocal IOLs; as such, some patients may need glasses when reading small print or looking at small objects.

Clinical studies with the AcrySof® ReSTOR® lens indicated that posterior capsule opacification (PCO), when present, developed earlier into clinically significant PCO. Prior to surgery, physicians should provide prospective patients with a copy of the Patient Information Brochure available from Alcon for this product informing them of possible risks and benefits associated with the AcrySof® IQ ReSTOR® IOLs.

Studies have shown that color vision discrimination is not adversely affected in individuals with the AcrySof® Natural IOL 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 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 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).