More patients get better outcomes with the IntraLase Method.1
IntraLase cannot be individualized.
IntraLase allows surgeons to tailor the corneal flap for each individual patient, and each individual eye.
IntraLase improves precision2 and outcomes1, whether you choose to have a standard or custom procedure.
IntraLase is not accurate.
IntraLase delivers micron-level accuracy, giving your doctor more control during the procedure and the ability to create a flap of precise size, shape, and depth—factors that are critical to a successful LASIK outcome.2
Leading doctors and teaching hospitals from around the world believe in IntraLase and use the IntraLase Method.
Patients prefer procedures using a microkeratome blade.
More patients (81%), when given a choice, chose the IntraLase Method over a microkeratome blade.3
Millions of IntraLase procedures have been safely performed.
The IntraLase Method takes much longer to perform than a microkeratome procedure.
The IntraLase Method takes approximately 15-20 seconds per eye and a total of 10 minutes for the entire LASIK procedure, which is comparable to—and sometimes faster than—procedures using a microkeratome.
IntraLase is the most sophisticated and accurate technology for corneal flap creation available today and has given many patients greater confidence and assurance in choosing laser vision correction.
REFERENCES:
Tanna M, Schallhorn S, Hettinger K. Femtosecond laser versus mechanical microkeratome: a retrospective comparison of visual outcomes at 3 months. J Refract Surg. 2009;25:1-4.
Stonecipher K, Ignacio TS, Stonecipher M. Advances in refractive surgery: microkeratome and femtosecond laser flap creation in relation to safety, efficacy, predictability, and biomechanical stability. Curr Opin Ophthalmol. 2006;17(4):368-372.
Mahdavi S. IntraLase: coming of age. Cataract Refract Surg Today. 2005:117-120.
SUMMARY OF SAFETY INFORMATION
The FS and iFS Laser systems are ophthalmic surgical lasers indicated for use in patients undergoing surgery or treatment requiring the initial lamellar resection of the cornea. Contraindications may include corneal edema, glaucoma, and keratoconus. Risks and complications may include corneal pain, flap tearing, and epithelial ingrowth. Consult with your eye care professional for a complete listing of contraindications and risks. US Federal law restricts this device to sale, distribution, and use by or on the order of a physician or other licensed eye care practitioner.
Unless otherwise specified, all product names appearing in this Internet site are trademarks owned by or licensed to Abbott Laboratories, its subsidiaries or affiliates. No use of any Abbott trademark, trade name, or trade dress in this site may be made without the prior written authorization of Abbott Laboratories, except to identify the product or services of the company. 2008.08.29-IL595 Rev. A
