K243940
- 510(k) number
- K243940
- Device name
- VITA YZ Multi Translucent
- Applicant
- Vita Zahnfabrik H.Rauter GmbH & Co. DE
- Product code
- EIH — Powder, Porcelain
- Decision date
- 2025-02-21
- Date received
- 2024-12-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 2.9 MB · U.S. public domain
Also available from FDA: K243940.pdf
Official FDA record: K243940
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.