ClearanceBrief
510(k) K241972 ยท DZE Implant, Endosseous, Root-Form

BLUEDIAMOND IMPLANT

ApplicantMegagen Implant Co., Ltd., Deagu, KR
DecisionSubstantially Equivalent, Dec 27, 2024
ReceivedJul 5, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K241972

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.