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 | 14 | Patient |
| 2024 | Swelling/ Edema | 2 | Patient |
| 2024 | Pain | 24 | Patient |
| 2024 | Numbness | 8 | Patient |
| 2024 | Insufficient Information | 4 | Patient |
| 2024 | Foreign Body In Patient | 4 | Patient |
| 2024 | Fistula | 12 | Patient |
| 2024 | Failure of Implant | 807 | Patient |
| 2024 | Bone Fracture(s) | 4 | Patient |
| 2024 | Abscess | 7 | Patient |
| 2024 | Premature Separation | 10 | Device |
| 2024 | Osseointegration Problem | 4 | Device |
| 2024 | Migration | 4 | Device |
| 2024 | Mechanical Problem | 2 | Device |
| 2024 | Malposition of Device | 1 | Device |
| 2024 | Loss of Osseointegration | 88 | Device |
| 2024 | Insufficient Information | 4 | Device |
| 2024 | Fracture | 13 | Device |
| 2024 | Failure to Osseointegrate | 518 | Device |
| 2024 | Difficult to Remove | 2 | Device |
| 2024 | Difficult to Insert | 2 | Device |
| 2024 | Defective Device | 2 | Device |
| 2024 | Adverse Event Without Identified Device or Use Problem | 19 | Device |
| 2024 | Activation, Positioning or Separation Problem | 2 | Device |
| 2023 | Unspecified Infection | 24 | Patient |
| 2023 | Pain | 74 | Patient |
| 2023 | Numbness | 12 | Patient |
| 2023 | Insufficient Information | 1 | Patient |
| 2023 | Foreign Body In Patient | 2 | Patient |
| 2023 | Fistula | 2 | Patient |
| 2023 | Failure of Implant | 829 | Patient |
| 2023 | Bone Fracture(s) | 2 | Patient |
| 2023 | Abscess | 2 | Patient |
| 2023 | Premature Separation | 3 | Device |
| 2023 | Patient Device Interaction Problem | 18 | Device |
| 2023 | Osseointegration Problem | 53 | Device |
| 2023 | Migration | 2 | Device |
| 2023 | Mechanical Problem | 1 | Device |
| 2023 | Material Deformation | 8 | Device |
| 2023 | Loss of Osseointegration | 122 | Device |
| 2023 | Insufficient Information | 1 | Device |
| 2023 | Fracture | 18 | Device |
| 2023 | Failure to Osseointegrate | 564 | Device |
| 2023 | Difficult to Insert | 2 | Device |
| 2023 | Adverse Event Without Identified Device or Use Problem | 10 | Device |
| 2022 | Unspecified Infection | 9 | Patient |
| 2022 | Pain | 27 | Patient |
| 2022 | Numbness | 10 | Patient |
| 2022 | Insufficient Information | 2 | Patient |
| 2022 | Fistula | 2 | Patient |
| 2022 | Failure of Implant | 139 | Patient |
| 2022 | Bone Fracture(s) | 2 | Patient |
| 2022 | Patient Device Interaction Problem | 2 | Device |
| 2022 | Osseointegration Problem | 59 | Device |
| 2022 | Material Deformation | 4 | Device |
| 2022 | Loss of Osseointegration | 86 | Device |
| 2022 | Insufficient Information | 4 | Device |
| 2022 | Fracture | 14 | Device |
| 2022 | Failure to Osseointegrate | 585 | Device |
| 2022 | Defective Device | 2 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 20 | Device |
| 2021 | Failure of Implant | 15 | Patient |
| 2021 | Bone Fracture(s) | 1 | Patient |
| 2021 | Patient Device Interaction Problem | 2 | Device |
| 2021 | Osseointegration Problem | 3 | Device |
| 2021 | Mechanical Problem | 1 | Device |
| 2021 | Loss of Osseointegration | 2 | Device |
| 2021 | Fracture | 1 | Device |
| 2021 | Failure to Osseointegrate | 52 | Device |
| 2021 | Adverse Event Without Identified Device or Use Problem | 1 | Device |
| 2020 | Failure of Implant | 2 | Patient |
| 2020 | Failure to Osseointegrate | 14 | Device |