ENDOSSEOUS DENTAL IMPLANT
This device is manufactured by NOBEL BIOCARE USA.
The following problems were reported about this device:
| Year | Description | Events/year | Type |
|---|---|---|---|
| 2024 | Unspecified Infection | 6 | Patient |
| 2024 | Pain | 4 | Patient |
| 2024 | Inflammation | 2 | Patient |
| 2024 | Failure of Implant | 226 | Patient |
| 2024 | Abscess | 6 | Patient |
| 2024 | Premature Separation | 2 | Device |
| 2024 | Mechanical Problem | 2 | Device |
| 2024 | Loss of Osseointegration | 22 | Device |
| 2024 | Flaked | 2 | Device |
| 2024 | Failure to Osseointegrate | 138 | Device |
| 2024 | Difficult to Insert | 4 | Device |
| 2024 | Device Markings/Labelling Problem | 4 | Device |
| 2024 | Device Damaged by Another Device | 2 | Device |
| 2024 | Adverse Event Without Identified Device or Use Problem | 6 | Device |
| 2024 | Activation, Positioning or Separation Problem | 6 | Device |
| 2023 | Unspecified Infection | 10 | Patient |
| 2023 | Pain | 18 | Patient |
| 2023 | Numbness | 4 | Patient |
| 2023 | Insufficient Information | 2 | Patient |
| 2023 | Foreign Body In Patient | 2 | Patient |
| 2023 | Fistula | 6 | Patient |
| 2023 | Failure of Implant | 237 | Patient |
| 2023 | Separation Failure | 2 | Device |
| 2023 | Patient Device Interaction Problem | 14 | Device |
| 2023 | Osseointegration Problem | 14 | Device |
| 2023 | Migration | 4 | Device |
| 2023 | Mechanical Problem | 2 | Device |
| 2023 | Material Deformation | 2 | Device |
| 2023 | Loss of Osseointegration | 34 | Device |
| 2023 | Insufficient Information | 2 | Device |
| 2023 | Failure to Osseointegrate | 163 | Device |
| 2023 | Device Markings/Labelling Problem | 4 | Device |
| 2023 | Adverse Event Without Identified Device or Use Problem | 6 | Device |
| 2022 | Unspecified Infection | 2 | Patient |
| 2022 | Pain | 6 | Patient |
| 2022 | Failure of Implant | 37 | Patient |
| 2022 | Osseointegration Problem | 12 | Device |
| 2022 | Loss of Osseointegration | 16 | Device |
| 2022 | Insufficient Information | 2 | Device |
| 2022 | Failure to Osseointegrate | 136 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 12 | Device |
| 2021 | Failure of Implant | 6 | Patient |
| 2021 | Bone Fracture(s) | 2 | Patient |
| 2021 | Failure to Osseointegrate | 6 | Device |
| 2021 | Adverse Event Without Identified Device or Use Problem | 2 | Device |
| 2019 | Failure of Implant | 1 | Patient |
| 2019 | Failure to Osseointegrate | 2 | Device |