K252343
- 510(k) number
- K252343
- Device name
- Atlantis® Abutments in Titanium
- Applicant
- Dentsply Sirona PA · US
- Product code
- NHA — Abutment, Implant, Dental, Endosseous
- Decision date
- 2025-12-09
- Date received
- 2025-07-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
510(k) Summary (official FDA PDF): K252343.pdf
Official FDA record: K252343
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.