K243103
- 510(k) number
- K243103
- Device name
- Denture Base
- Applicant
- Riton 3D Technology Co., Ltd. CN
- Product code
- EBI — Resin, Denture, Relining, Repairing, Rebasing
- Decision date
- 2024-12-23
- Date received
- 2024-09-30
- 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: K243103.pdf
Official FDA record: K243103
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.