Neodent USA, Inc. · Class II · Cleared Aug 22, 2014
| K-number | K133592 |
| Device name | NEODENT IMPLANT SYSTEM, TITAMAX TI EX ACQUA AND TI DRIVE ACQUA, TITAMAX SMART EX ACQUA AND DRIVE SMART ACQUA, TITAMAX CM |
| Applicant | Neodent USA, Inc. |
| Product code | DZE |
| Device class | Class II |
| Decision date | Aug 22, 2014 |
| Decision | Substantially Equivalent |
| Regulation | 872.3640 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov