ClearanceBrief
510(k) K102635 ยท DZE Implant, Endosseous, Root-Form

APOLONIA LASER IMPLANT SYSTEM

ApplicantCsm Implant Co., Ltd., Brea CA, US
DecisionSubstantially Equivalent, Mar 22, 2011
ReceivedSep 13, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K102635

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.