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This article was originally published in The Gray Sheet
FDA approves company's CeeOn Edge 911A intraocular lens April 16 for patients whose cataractous lens has been surgically removed. A 434-patient, 15-center clinical trial evaluating the CeeOn Edge showed a low incidence of posterior capsular opacification due to the square-edged design of the lens, Pharmacia says. Of 320 patients who completed one-year follow-up, 97% achieved visual acuity of 20/40 or better
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