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 | 15 | Patient |
| 2024 | Pain | 6 | Patient |
| 2024 | Numbness | 2 | Patient |
| 2024 | Foreign Body In Patient | 5 | Patient |
| 2024 | Fistula | 1 | Patient |
| 2024 | Failure of Implant | 212 | Patient |
| 2024 | Abscess | 2 | Patient |
| 2024 | Migration | 1 | Device |
| 2024 | Loss of Osseointegration | 32 | Device |
| 2024 | Failure to Osseointegrate | 144 | Device |
| 2024 | Difficult to Insert | 2 | Device |
| 2024 | Adverse Event Without Identified Device or Use Problem | 3 | Device |
| 2023 | Unspecified Infection | 21 | Patient |
| 2023 | Pain | 18 | Patient |
| 2023 | Numbness | 7 | Patient |
| 2023 | Failure of Implant | 322 | Patient |
| 2023 | Bone Fracture(s) | 1 | Patient |
| 2023 | Abscess | 3 | Patient |
| 2023 | Patient Device Interaction Problem | 9 | Device |
| 2023 | Osseointegration Problem | 19 | Device |
| 2023 | Malposition of Device | 2 | Device |
| 2023 | Loss of Osseointegration | 37 | Device |
| 2023 | Fracture | 2 | Device |
| 2023 | Failure to Osseointegrate | 245 | Device |
| 2023 | Difficult to Insert | 1 | Device |
| 2023 | Adverse Event Without Identified Device or Use Problem | 3 | Device |
| 2022 | Unspecified Infection | 11 | Patient |
| 2022 | Pain | 11 | Patient |
| 2022 | Insufficient Information | 3 | Patient |
| 2022 | Failure of Implant | 114 | Patient |
| 2022 | Bone Fracture(s) | 2 | Patient |
| 2022 | Osseointegration Problem | 11 | Device |
| 2022 | Material Deformation | 1 | Device |
| 2022 | Loss of Osseointegration | 37 | Device |
| 2022 | Insufficient Information | 5 | Device |
| 2022 | Fracture | 3 | Device |
| 2022 | Failure to Osseointegrate | 167 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 4 | Device |
| 2021 | Unspecified Infection | 4 | Patient |
| 2021 | Pain | 2 | Patient |
| 2021 | Failure of Implant | 27 | Patient |
| 2021 | Osseointegration Problem | 1 | Device |
| 2021 | Loss of Osseointegration | 6 | Device |
| 2021 | Failure to Osseointegrate | 31 | Device |
| 2021 | Adverse Event Without Identified Device or Use Problem | 1 | Device |
| 2020 | Failure of Implant | 14 | Patient |
| 2020 | Failure to Osseointegrate | 12 | Device |
| 2019 | Failure of Implant | 14 | Patient |
| 2019 | Loss of Osseointegration | 40 | Device |
| 2019 | Fracture | 1 | Device |
| 2019 | Failure to Osseointegrate | 75 | Device |
| 2019 | Adverse Event Without Identified Device or Use Problem | 2 | Device |
| 2018 | Loss of Osseointegration | 4 | Device |
| 2018 | Failure to Osseointegrate | 7 | Device |