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 | 33 | Patient |
| 2024 | Pain | 42 | Patient |
| 2024 | Numbness | 5 | Patient |
| 2024 | Insufficient Information | 6 | Patient |
| 2024 | Foreign Body In Patient | 4 | Patient |
| 2024 | Fistula | 2 | Patient |
| 2024 | Failure of Implant | 693 | Patient |
| 2024 | Bone Fracture(s) | 2 | Patient |
| 2024 | Abscess | 4 | Patient |
| 2024 | Premature Separation | 6 | Device |
| 2024 | Osseointegration Problem | 6 | Device |
| 2024 | Migration | 2 | Device |
| 2024 | Loss of Osseointegration | 110 | Device |
| 2024 | Insufficient Information | 5 | Device |
| 2024 | Fracture | 2 | Device |
| 2024 | Failure to Osseointegrate | 431 | Device |
| 2024 | Device Markings/Labelling Problem | 2 | Device |
| 2024 | Adverse Event Without Identified Device or Use Problem | 8 | Device |
| 2023 | Unspecified Infection | 34 | Patient |
| 2023 | Sinus Perforation | 2 | Patient |
| 2023 | Pain | 98 | Patient |
| 2023 | Numbness | 30 | Patient |
| 2023 | Insufficient Information | 2 | Patient |
| 2023 | Implant Pain | 4 | Patient |
| 2023 | Foreign Body In Patient | 2 | Patient |
| 2023 | Fistula | 2 | Patient |
| 2023 | Failure of Implant | 789 | Patient |
| 2023 | Bone Fracture(s) | 2 | Patient |
| 2023 | Abscess | 2 | Patient |
| 2023 | Separation Failure | 2 | Device |
| 2023 | Premature Separation | 4 | Device |
| 2023 | Patient Device Interaction Problem | 8 | Device |
| 2023 | Osseointegration Problem | 34 | Device |
| 2023 | Missing Information | 2 | Device |
| 2023 | Migration | 4 | Device |
| 2023 | Malposition of Device | 2 | Device |
| 2023 | Loss of Osseointegration | 128 | Device |
| 2023 | Insufficient Information | 2 | Device |
| 2023 | Fracture | 2 | Device |
| 2023 | Failure to Osseointegrate | 545 | Device |
| 2023 | Difficult to Insert | 2 | Device |
| 2023 | Adverse Event Without Identified Device or Use Problem | 14 | Device |
| 2022 | Unspecified Infection | 11 | Patient |
| 2022 | Pain | 49 | Patient |
| 2022 | Numbness | 14 | Patient |
| 2022 | Failure of Implant | 218 | Patient |
| 2022 | Bone Fracture(s) | 4 | Patient |
| 2022 | Separation Failure | 2 | Device |
| 2022 | Patient Device Interaction Problem | 2 | Device |
| 2022 | Osseointegration Problem | 70 | Device |
| 2022 | Material Deformation | 2 | Device |
| 2022 | Malposition of Device | 6 | Device |
| 2022 | Loss of Osseointegration | 124 | Device |
| 2022 | Fracture | 5 | Device |
| 2022 | Failure to Osseointegrate | 504 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 10 | Device |
| 2021 | Unspecified Infection | 2 | Patient |
| 2021 | Sinus Perforation | 2 | Patient |
| 2021 | Pain | 4 | Patient |
| 2021 | Failure of Implant | 26 | Patient |
| 2021 | Osseointegration Problem | 2 | Device |
| 2021 | Loss of Osseointegration | 8 | Device |
| 2021 | Failure to Osseointegrate | 66 | Device |
| 2020 | Failure of Implant | 6 | Patient |
| 2020 | Patient Device Interaction Problem | 2 | Device |
| 2020 | Failure to Osseointegrate | 6 | Device |