ClearanceBrief
510(k) K202792 ยท NXC Aligner, Sequential

BRIUS Clear Aligners

ApplicantBrius Technologies, Inc., Carrollton TX, US
DecisionSubstantially Equivalent, Jan 22, 2021
ReceivedSep 22, 2020
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K202792

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.