Submission Details
| 510(k) Number | K240688 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | March 13, 2024 |
| Decision Date | June 20, 2024 |
| Days to Decision | 99 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
K240688 is an FDA 510(k) clearance for the RODIN Titan 3D Resin, a Resin, Denture, Relining, Repairing, Rebasing (Class II — Special Controls, product code EBI), submitted by Belport Company, Inc., Gingi-Pak (Brea, US). The FDA issued a Cleared decision on June 20, 2024, 99 days after receiving the submission on March 13, 2024. This device falls under the Dental review panel. Regulated under 21 CFR 872.3760.
| 510(k) Number | K240688 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | March 13, 2024 |
| Decision Date | June 20, 2024 |
| Days to Decision | 99 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
| Product Code | EBI — Resin, Denture, Relining, Repairing, Rebasing |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 872.3760 |