K261166
- 510(k) number
- K261166
- Device name
- DIA-CEM
- Applicant
- DiaDent Group International KR
- Product code
- EMA — Cement, Dental
- Decision date
- 2026-07-09
- Date received
- 2026-04-09
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K261166.pdf
Official FDA record: K261166
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.