K260918
- 510(k) number
- K260918
- Device name
- Zolid Lunaris
- Applicant
- Amann Girrbach AG AT
- Product code
- EIH — Powder, Porcelain
- Decision date
- 2026-06-29
- Date received
- 2026-03-19
- 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: K260918.pdf
Official FDA record: K260918
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.