Dentimax, Inc. · Class II · Cleared Sep 24, 2025
| K-number | K251206 |
| Device name | Digital X-Ray DentiMax Pro Imaging System |
| Applicant | Dentimax, Inc. |
| Product code | MUH |
| Device class | Class II |
| Decision date | Sep 24, 2025 |
| Decision | Substantially Equivalent |
| Regulation | 872.1800 |
The FDA summary PDF for this submission is not available in machine-readable form — common for older clearances. View on FDA's site →
View the full FDA submission: accessdata.fda.gov