| Device Type ID | 1108 |
| Device Name | Instruments, Dental Hand |
| Regulation Description | Dental Hand Instrument. |
| Regulation Medical Specialty | Dental |
| Review Panel | Dental |
| Premarket Review | Office Of Device Evaluation (ODE) Division Of Anesthesiology, General Hospital, Infection Control, And Dental Devices (DAGRID) Dental Devices Branch (DEDB) |
| Submission Type | 510(K) Exempt |
| CFR Regulation Number | 872.4565 [🔎] |
| FDA Device Classification | Class 1 Medical Device |
| Product Code | DZN |
| GMP Exempt | No |
| Summary MR | Eligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Not Third Party Eligible |
|
| Device Type ID | 1108 |
| Device | Instruments, Dental Hand |
| Product Code | DZN |
| FDA Device Classification | Class 1 Medical Device |
| Regulation Description | Dental Hand Instrument. |
| CFR Regulation Number | 872.4565 [🔎] |
| Device Problems | |
|---|---|
Break | 26 |
Tip | 14 |
Material Integrity Problem | 5 |
Flaked | 5 |
Peeled / Delaminated | 5 |
Material Fragmentation | 1 |
Adverse Event Without Identified Device Or Use Problem | 1 |
| Total Device Problems | 57 |
| Recalls | |||
|---|---|---|---|
| Manufacturer | Recall Class | Date Posted | |
| 1 | Ultradent Products, Inc. | II | Jan-05-2016 |