The LASIK BlogInformation about LASIK and Custom LASIK ProceduresNidek Seeks Hyperopia Approval from FDA- January 30, 2008 NIDEK Hyperopia Clinical Study Update & Future FDA Studies -Fremont, CA USA, May 4th, 2004- NIDEK, Inc. announced today that it has completed and submitted 3-month clinical data for its new hyperopia study to the FDA. This marks an important milestone in the study process, as additional treatment eyes will be initiated in the study protocol effective immediately. NIDEK also received approval from the FDA to expand the clinical study to 300 eyes under the current treatment protocol. The...http://www.globallaservision.com/blog/index.php?/archives/188-Nidek-Seeks-Hyperopia-Approv... Study of Indication and use of Nidek in treating myopia and astigmatism- January 30, 2008 The NIDEK EC-5000 Excimer Laser System (including EC-5000CXCXII) has been approved for use in the United States to perform photorefractive keratectomy (PRK) for the reduction or elimination of myopia in the low, moderate or high ranges (-0.75 to -13.00 D), spherical equivalent at the spectacle plane, uncomplicated by refractive astigmatism (i.e. equal or less than 0.75 D in any meridian), and of moderate myopia with astigmatism from -1.00 to -8.00 D spherical equivalent with astigmatism from...http://www.globallaservision.com/blog/index.php?/archives/187-Study-of-Indication-and-use-... |