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 | Pain | 2 | Patient |
| 2024 | Fistula | 4 | Patient |
| 2024 | Failure of Implant | 294 | Patient |
| 2024 | Bone Fracture(s) | 2 | Patient |
| 2024 | Abscess | 12 | Patient |
| 2024 | Naturally Worn | 2 | Device |
| 2024 | Loss of Osseointegration | 38 | Device |
| 2024 | Fracture | 2 | Device |
| 2024 | Failure to Osseointegrate | 175 | Device |
| 2024 | Difficult to Insert | 2 | Device |
| 2024 | Device Markings/Labelling Problem | 2 | Device |
| 2024 | Adverse Event Without Identified Device or Use Problem | 12 | Device |
| 2024 | Activation, Positioning or Separation Problem | 6 | Device |
| 2023 | Unspecified Infection | 8 | Patient |
| 2023 | Pain | 58 | Patient |
| 2023 | Numbness | 18 | Patient |
| 2023 | Insufficient Information | 5 | Patient |
| 2023 | Foreign Body In Patient | 2 | Patient |
| 2023 | Fistula | 1 | Patient |
| 2023 | Failure of Implant | 399 | Patient |
| 2023 | Bone Fracture(s) | 4 | Patient |
| 2023 | Abscess | 2 | Patient |
| 2023 | Premature Separation | 6 | Device |
| 2023 | Patient Device Interaction Problem | 20 | Device |
| 2023 | Osseointegration Problem | 14 | Device |
| 2023 | Migration | 4 | Device |
| 2023 | Loss of Osseointegration | 29 | Device |
| 2023 | Insufficient Information | 3 | Device |
| 2023 | Fracture | 9 | Device |
| 2023 | Failure to Osseointegrate | 296 | Device |
| 2023 | Difficult to Insert | 3 | Device |
| 2023 | Device Markings/Labelling Problem | 2 | Device |
| 2023 | Adverse Event Without Identified Device or Use Problem | 12 | Device |
| 2022 | Unspecified Infection | 8 | Patient |
| 2022 | Pain | 13 | Patient |
| 2022 | Numbness | 2 | Patient |
| 2022 | Insufficient Information | 4 | Patient |
| 2022 | Failure of Implant | 79 | Patient |
| 2022 | Separation Failure | 2 | Device |
| 2022 | Osseointegration Problem | 42 | Device |
| 2022 | Material Deformation | 4 | Device |
| 2022 | Malposition of Device | 2 | Device |
| 2022 | Loss of Osseointegration | 16 | Device |
| 2022 | Insufficient Information | 10 | Device |
| 2022 | Fracture | 9 | Device |
| 2022 | Failure to Osseointegrate | 281 | Device |
| 2022 | Device Markings/Labelling Problem | 2 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 13 | Device |
| 2021 | Failure of Implant | 4 | Patient |
| 2021 | Patient Device Interaction Problem | 2 | Device |
| 2021 | Failure to Osseointegrate | 13 | Device |
| 2020 | Pain | 2 | Patient |
| 2020 | Failure of Implant | 2 | Patient |
| 2020 | Failure to Osseointegrate | 2 | Device |
| 2020 | Device Markings/Labelling Problem | 2 | Device |