ClearanceBrief
510(k) K231411 ยท NHA Abutment, Implant, Dental, Endosseous

INNO SLA Submerged Hybrid Ti-Base System

ApplicantCowellmedi Co., Ltd., Busan, KR
DecisionSubstantially Equivalent, Dec 20, 2023
ReceivedMay 16, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K231411

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.