K240688
- 510(k) number
- K240688
- Device name
- RODIN Titan 3D Resin
- Applicant
- Belport Company, Inc., Gingi-Pak CA · US
- Product code
- EBI — Resin, Denture, Relining, Repairing, Rebasing
- Decision date
- 2024-06-20
- Date received
- 2024-03-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K240688.pdf
Official FDA record: K240688
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.