K241151
- 510(k) number
- K241151
- Device name
- LUXEN 5G
- Applicant
- Dentalmax Co., Ltd. KR
- Product code
- EIH — Powder, Porcelain
- Decision date
- 2024-09-30
- Date received
- 2024-04-25
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K241151.pdf
Official FDA record: K241151
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.