K252320
- 510(k) number
- K252320
- Device name
- SIMDA Abutments
- Applicant
- Simda Co., Ltd. KR
- Product code
- NHA — Abutment, Implant, Dental, Endosseous
- Decision date
- 2025-12-18
- Date received
- 2025-07-25
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K252320.pdf
Official FDA record: K252320
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.