K250826
- 510(k) number
- K250826
- Device name
- Multi M Series
- Applicant
- Dmax Co., Ltd. KR
- Product code
- EIH — Powder, Porcelain
- Decision date
- 2025-06-12
- Date received
- 2025-03-18
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K250826.pdf
Official FDA record: K250826
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.