ClearanceBrief
510(k) K253999 ยท NHA Abutment, Implant, Dental, Endosseous

Universal Base ASC Engaging; Universal Base ASC Non-Engaging; Universal Base MUA ASC; Temporary Abutment Engaging and Non-Engaging; Healing Abutment Conical Connection; Omnigrip Clinical Screw Titanium; Omnigrip Prosthetic Screw

ApplicantNobel Biocare AB, Goteborg, SE
DecisionSubstantially Equivalent, Aug 6, 2026
ReceivedDec 15, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K253999

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.