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 |