CustomVue Monovision LASIK, Approved by the FDA
Filed in archive Treatment by Gloria Gamat on July 16, 2007

[CustomVue Monovision LASIK produces monovision correction in nearsighted (myopic) adults, with or without astigmatism, ages 40 years or older with normal age-related loss of ability to focus on near objects (presbyopia).]
Now, the device has been cleared for marketing by the FDA.
[LASIK, or laser in-situ keratomileusis, is a procedure in which the surgeon cuts a flap in the outer layers of the cornea, removes a small amount of the tissue beneath it with the laser, and then replaces the flap.]
Manufactured by AMO/VISX Inc., based in Santa Clara
, California, CustomVue Monovision LASIK has been approved by the FDA based on the review of a clinical study of safety and effectiveness outcomes submitted by the company. Find more details from the full report.
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