ZEISS Gains FDA Approval for Visumax® SMILE Vision Correction Procedure

18 Sept 2016
Lois Manton-O'Byrne, PhD
Executive Editor

Industry news

The Medical Technology Business Group of ZEISS announces the introduction in the US of the VisuMax® Small Incision Lenticule Extraction (SMILE) procedure, the latest advancement in refractive surgery for the correction of myopia. SMILE, a minimally-invasive corneal refractive procedure, performed on the ZEISS VisuMax femtosecond laser, is currently available in approximately 500 clinics in 61 countries around the world.

More than a half a million SMILE procedures have been performed internationally since its introduction in 2011 with extensive study results demonstrating high levels of safety and effectiveness. This next evolution in refractive technology is now available to US surgeons expanding the options for laser eye surgery that they can offer to their patients.

Pivotal study results submitted to the US FDA in ZEISS’ Pre-Market Approval (PMA) application demonstrated excellent visual acuity and refractive predictability outcomes for the 336 eyes treated at five investigational sites in the US. SMILE, a femtosecond laser-based, minimally-invasive vision correction procedure, is already established in global markets such as Europe, China, Australia, Canada and India.

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Clinical TrialsClinical Trials, an essential part of drug discovery process, assess the safety and effectiveness of a new medication or device in the pharmaceutical industry. Clinical Trials are a phased process (Phase 0, Phase I, Phase II, Phase III and Phase IV) which begins after initial preclinical testing.FDAThe Food and Drug Association (FDA) is an agency within the U.S. Department of Health and Human Services. Among other things, it is responsible for ensuring the safety, effectiveness and quality of drugs, vaccines and other biological products, and medical devices.
ZEISS Gains FDA Approval for Visumax® SMILE Vision Correction Procedure