Bonart Co., Ltd. · Class II · Cleared Aug 15, 2016
| K-number | K152125 |
| Device name | Oral Surgery System and Accessories |
| Applicant | Bonart Co., Ltd. |
| Product code | DZI |
| Device class | Class II |
| Decision date | Aug 15, 2016 |
| Decision | Substantially Equivalent |
| Regulation | 872.4120 |
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