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U.S. Department of Health and Human Services

Medical Devices

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Akreos® Posterior Chamber Intraocular Lens - P060022

photo of Akreos® Posterior Chamber Intraocular Lens - P060022This is a brief overview of information related to FDA’s approval to market this product. See the links below to the Summary of Safety and Effectiveness Data (SSED) and product labeling for more complete information on this product, its indications for use, and the basis for FDA’s approval.


Product Name: Akreos Posterior Chamber Intraocular Lens
PMA Applicant: Bausch & Lomb
Address: 1400 North Goodman Street, Rochester, NY 14609
Approval Date: September 5, 2008
Approval Letter: http://www.accessdata.fda.gov/cdrh_docs/pdf6/p060022a.pdf

What is it? Akreos ® posterior chamber intraocular lens (IOL) is an artificial lens used to restore vision and replace the natural lens of the eye after it is removed during cataract surgery. A cataract is a gradual thickening, hardening and clouding of the eye's lens, resulting in loss of vision. Cataracts are often the result of aging, but can have other causes.

How does it work? Akreos® acts in place of the healthy eye lens to correctly focus light on the retina and restore vision.

When is it used? Akreos® is used to restore vision in adult patients who have had a cataract removed.

What will it accomplish? Akreos® restores vision by acting as a substitute for the removed natural lens.

When should it not be used? Akreos® should not be implanted when the IOL may make worse an existing condition, interfere with the diagnosis or the treatment of a condition, or present a risk to the sight of the patient.

Additional information: The Summary of Safety and Effectiveness and labeling will be available at: http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cftopic/pma/pma.cfm?num=p060022