INTACS
Intacs®, is the first non-laser surgical product approved by the U.S. Food and Drug Administration for vision correction. These tiny transparent ring segments can efficiently correct mild to moderate amounts of keratoconus.
Procedure Intacs® are implanted into the periphery of the cornea. The channels for the Intacs® segments are created using the IntraLase® laser and the segments are placed into position. By increasing the volume in the peripheral cornea, there is a flattening in the central portion of the cornea. Following insertion of Intacs®, a microscopic suture (thinner than a human hair) is used to close the incision.
The Intacs® procedure is highly effective, with over 80 percent of patients achieving 20/20 vision and over 50 percent of patients seeing better than 20/20!
Intacs® are designed to be permanent; however, the segments can be removed. Removal allows the eye to virtually return to its natural state prior to surgery. This attribute and the fact that the surgery does not involve altering the central cornea (as with laser vision correction), make Intacs® a unique technology for vision correction.
Recovery Visual recovery is very rapid. Patients can return to most normal activities on the same day as surgery (see post-operative instruction sheet). Patients routinely go to work the next day. The results of the recent FDA clinical trials demonstrate long-term stability.
Benefits The benefits of Intacs® include:
- FDA-approved
- Non-laser procedure
- Rapid improvement in vision
- Maintenance-free correction
- Excellent visual results
- Tissue is not removed from the central cornea, the region most critical to your vision
- Intacs® can be removed or replaced
Are You a Candidate for Intacs®? You may qualify for Intacs® if:
- You have a history of keratoconus
- You have healthy eyes, free from disease or injuries
- You have had stable vision for one year
- You are at least 21 years of age
For more information about Intacs®, contact us today at 1.800.527.3745.