AcrySof® IQ ReSTOR® +3.0 D
Multifocal IOL

Recommend AcrySof® IQ ReSTOR® +3.0 D IOL with a pupil-adaptive design for your appropriate patients who want:

  • A broad range of vision from 16 inches (40 cm) to distance
  • The greatest opportunity for spectacle independence
  • To engage in a variety of activities requiring near, intermediate and distant focal points

Designed to reduce spectacle dependence at all distances for the broadest range of vision,* this advanced IOL can help your patients refocus on the activities they love1:

  • Reading
  • Cooking
  • Playing cards
  • Watching TV
AcrySof® IQ ReSTOR® IOLs provide the broadest range of vision
*Broadest range of vision across all Alcon® IOLs approved in the United States.

AcrySof® IQ ReSTOR® +3.0 D IOL Data Support

Spectacle independence1

With the AcrySof® IQ ReSTOR®
+3.0 D IOL, eight out of 10 patients reported complete freedom from glasses six months after surgery.1

AcrySof® IQ ReSTOR® +3.0 D IOL spectacle-independence

Patient satisfaction1

More than 93% of patients surveyed indicated they would have the AcrySof® IQ ReSTOR® +3.0 D IOL implanted again.1

AcrySof® IQ ReSTOR® +3.0 D IOL patient satisfaction

AcrySof® IQ ReSTOR® +3.0 D IOL Defocus Curve1,2

Pupil-adaptive design is engineered to1:

  • Allocate light to the retina more like the natural eye
  • Deliver peak near vision at 40 cm
  • Provide excellent acuity (20-32 or better) at near, intermediate and distance
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

Simulated headlight images in Alcon model eye3
(5 mm pupil measured on the optikos MTF system)

AcrySof® IQ ReSTOR® +3.0 D IOL simulated headlight comparison

Visual disturbances1

In a six month post-op survey of AcrySof® IQ ReSTOR® +3.0 D IOL recipients, over
85% reported “None/Mild” difficulty with night vision.1


AcrySof® IQ ReSTOR® +3.0 D IOL product specifications

**None/Mild = 0-2, Moderate = 3-5, Severe = 6-7

Aim Multifocal
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).