Analysis of adverse events with use of orthodontic sequential aligners as reported in the manufacturer and user facility device experience database
Background: Sequential aligners (SAs) introduced about a decade ago, changed the practice of orthodontics as we knew it but the adverse events and reactions (AER) associated with SA is not known. The Food and Drug Administration's Manufacturer and User Facility Device Experience (MAUDE) databas...
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Wolters Kluwer Medknow Publications,
2015-01-01T00:00:00Z.
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A1234.567 |
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