Submission Details
| 510(k) Number | K241729 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | June 14, 2024 |
| Decision Date | March 18, 2025 |
| Days to Decision | 277 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
K241729 is an FDA 510(k) clearance for the Hard Splint & Thermo-Adaptive Splint, a Mouthguard, Prescription, submitted by Whip Mix Corporation (Louisville, US). The FDA issued a Cleared decision on March 18, 2025, 277 days after receiving the submission on June 14, 2024. This device falls under the Dental review panel.
| 510(k) Number | K241729 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | June 14, 2024 |
| Decision Date | March 18, 2025 |
| Days to Decision | 277 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
| Product Code | MQC — Mouthguard, Prescription |
| Device Class | — |