FDA Approves CustomVue Monovision LASIK

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Friday, July 13, 2007

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Medical News Today

The U.S. Food and Drug Administration approved for marketing the first LASIK device designed for treating one eye to see far away objects and the other eye for close-up vision.

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If standard keratometry and biometry measurements are used to calculate the IOL power in a patient who has previously had myopic LASIK, the selected IOL power will most likely be too high.
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FDA Approves CustomVue Monovision LASIK

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If standard keratometry and biometry measurements are used to calculate the IOL power in a patient who has previously had myopic LASIK, the selected IOL power will most likely be too high.

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