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 | 19 | Patient |
| 2024 | Pain | 12 | Patient |
| 2024 | Inflammation | 4 | Patient |
| 2024 | Foreign Body In Patient | 5 | Patient |
| 2024 | Fistula | 2 | Patient |
| 2024 | Failure of Implant | 404 | Patient |
| 2024 | Abscess | 6 | Patient |
| 2024 | Premature Separation | 2 | Device |
| 2024 | Osseointegration Problem | 7 | Device |
| 2024 | Migration | 5 | Device |
| 2024 | Mechanical Problem | 1 | Device |
| 2024 | Loss of Osseointegration | 146 | Device |
| 2024 | Fracture | 5 | Device |
| 2024 | Failure to Osseointegrate | 209 | Device |
| 2024 | Adverse Event Without Identified Device or Use Problem | 2 | Device |
| 2023 | Unspecified Infection | 18 | Patient |
| 2023 | Pain | 23 | Patient |
| 2023 | Numbness | 4 | Patient |
| 2023 | Insufficient Information | 2 | Patient |
| 2023 | Inflammation | 3 | Patient |
| 2023 | Foreign Body In Patient | 3 | Patient |
| 2023 | Failure of Implant | 396 | Patient |
| 2023 | Bone Fracture(s) | 7 | Patient |
| 2023 | Abscess | 2 | Patient |
| 2023 | Separation Failure | 2 | Device |
| 2023 | Patient Device Interaction Problem | 4 | Device |
| 2023 | Osseointegration Problem | 11 | Device |
| 2023 | Migration | 3 | Device |
| 2023 | Loss of Osseointegration | 60 | Device |
| 2023 | Insufficient Information | 2 | Device |
| 2023 | Fracture | 3 | Device |
| 2023 | Failure to Osseointegrate | 276 | Device |
| 2023 | Difficult to Insert | 3 | Device |
| 2023 | Device Markings/Labelling Problem | 2 | Device |
| 2023 | Adverse Event Without Identified Device or Use Problem | 8 | Device |
| 2022 | Unspecified Infection | 16 | Patient |
| 2022 | Pain | 11 | Patient |
| 2022 | Osteopenia/ Osteoporosis | 1 | Patient |
| 2022 | Numbness | 4 | Patient |
| 2022 | Failure of Implant | 114 | Patient |
| 2022 | Osseointegration Problem | 8 | Device |
| 2022 | Material Deformation | 2 | Device |
| 2022 | Loss of Osseointegration | 53 | Device |
| 2022 | Insufficient Information | 1 | Device |
| 2022 | Fracture | 5 | Device |
| 2022 | Failure to Osseointegrate | 212 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 7 | Device |
| 2021 | Failure of Implant | 11 | Patient |
| 2021 | Loss of Osseointegration | 5 | Device |
| 2021 | Fracture | 1 | Device |
| 2021 | Failure to Osseointegrate | 47 | Device |
| 2021 | Adverse Event Without Identified Device or Use Problem | 2 | Device |
| 2020 | Unspecified Infection | 2 | Patient |
| 2020 | Failure of Implant | 20 | Patient |
| 2020 | Osseointegration Problem | 4 | Device |
| 2020 | Loss of Osseointegration | 2 | Device |
| 2020 | Failure to Osseointegrate | 18 | Device |