The customer reported an infection while wearing the aligners, the customer was not able to provide the impacted tooth number.Medical intervention was required, and a root canal was performed.Aligner treatment was discontinued.For this event, the patient identifier is (b)(6) and the complaint number is (b)(4).
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Based on the information provided by the patient, there is no conclusive evidence that supports or opposes the fact that the aligners caused, contributed, or would likely cause or contribute to the reported event.This event is being filed as an mdr since the patient reported symptoms or physiological conditions related to a tooth infection.
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