Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
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On april 30 2007 visx incorporated became aware of a significant overcorrection in one eye of a patient who had recieved a wavefront-guided lasik treatment at a facility in ecuador.