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Adverse-event reports (MAUDE)

Read this first: MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line shows reporting volume for the average device in the same FDA product code — a reporting baseline, not a risk measure.

No adverse-event reports are linked to this device.

Recall history
InitiatedRecall #ClassStatusReasonQuantityLink basis
2024-11-22Z-0743-2025Class IIOpen, ClassifiedAttachments may not mate with the tooth as intended in the digital treatment design.Distribution: Product was distributed nationwide US, and internationally to Canada, Australia, and New Zealand.171 orderscode info di
Regulatory clearances

None linked.

Manufacturer compliance record
DateTypeOutcomeFacilityCitations
2014-03-27VAIVoluntary action indicated3M Unitek Corporation7
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