ClearanceBrief
510(k) K202942 ยท DZE Implant, Endosseous, Root-Form

Straumann 4 mm Short Implants

ApplicantStraumann USA, LLC, Andover MA, US
DecisionSubstantially Equivalent, Feb 8, 2021
ReceivedSep 30, 2020
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K202942

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.