Device Type ID | 1091 |
Device Name | Retainer, Screw Expansion, Orthodontic |
Regulation Description | Orthodontic Appliance And Accessories. |
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 | 872.5410 [🔎] |
FDA Device Classification | Class 1 Medical Device |
Product Code | DYJ |
GMP Exempt | No |
Summary MR | Eligible |
Implanted Device | No |
Life Support Device | No |
Third Party Review | Not Third Party Eligible |
|
Device Type ID | 1091 |
Device | Retainer, Screw Expansion, Orthodontic |
Product Code | DYJ |
FDA Device Classification | Class 1 Medical Device |
Regulation Description | Orthodontic Appliance And Accessories. |
CFR Regulation Number | 872.5410 [🔎] |
Device Problems | |
---|---|
Adverse Event Without Identified Device Or Use Problem | 9 |
Material Fragmentation | 1 |
Break | 1 |
Total Device Problems | 11 |
Recalls | |||
---|---|---|---|
Manufacturer | Recall Class | Date Posted | |
1 | Allesee Orthodontic Appliances | II | Apr-01-2014 |