ClearanceBrief
510(k) K192581 ยท LQZ Device, Jaw Repositioning

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ApplicantAdvanced Facialdontics, LLC, St James NY, US
DecisionSubstantially Equivalent, Jan 28, 2020
ReceivedSep 19, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K192581

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.