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 | 6 | Patient |
| 2024 | Pain | 15 | Patient |
| 2024 | Osteomyelitis | 2 | Patient |
| 2024 | Numbness | 12 | Patient |
| 2024 | Insufficient Information | 2 | Patient |
| 2024 | Foreign Body In Patient | 2 | Patient |
| 2024 | Failure of Implant | 367 | Patient |
| 2024 | Bone Fracture(s) | 2 | Patient |
| 2024 | Abscess | 2 | Patient |
| 2024 | Premature Separation | 4 | Device |
| 2024 | Osseointegration Problem | 4 | Device |
| 2024 | Material Deformation | 2 | Device |
| 2024 | Loss of Osseointegration | 83 | Device |
| 2024 | Insufficient Information | 2 | Device |
| 2024 | Fracture | 2 | Device |
| 2024 | Failure to Osseointegrate | 191 | Device |
| 2024 | Adverse Event Without Identified Device or Use Problem | 4 | Device |
| 2024 | Activation, Positioning or Separation Problem | 4 | Device |
| 2023 | Unspecified Infection | 17 | Patient |
| 2023 | Paresthesia | 1 | Patient |
| 2023 | Pain | 79 | Patient |
| 2023 | Numbness | 32 | Patient |
| 2023 | Insufficient Information | 2 | Patient |
| 2023 | Fistula | 2 | Patient |
| 2023 | Failure of Implant | 601 | Patient |
| 2023 | Bone Fracture(s) | 2 | Patient |
| 2023 | Abscess | 4 | Patient |
| 2023 | Premature Separation | 2 | Device |
| 2023 | Patient Device Interaction Problem | 15 | Device |
| 2023 | Osseointegration Problem | 50 | Device |
| 2023 | Migration | 1 | Device |
| 2023 | Mechanical Problem | 2 | Device |
| 2023 | Material Discolored | 4 | Device |
| 2023 | Material Deformation | 2 | Device |
| 2023 | Malposition of Device | 9 | Device |
| 2023 | Loss of Osseointegration | 159 | Device |
| 2023 | Insufficient Information | 2 | Device |
| 2023 | Fracture | 8 | Device |
| 2023 | Failure to Osseointegrate | 346 | Device |
| 2023 | Adverse Event Without Identified Device or Use Problem | 8 | Device |
| 2022 | Unspecified Infection | 6 | Patient |
| 2022 | Pain | 14 | Patient |
| 2022 | Numbness | 3 | Patient |
| 2022 | Foreign Body In Patient | 1 | Patient |
| 2022 | Failure of Implant | 105 | Patient |
| 2022 | Osseointegration Problem | 26 | Device |
| 2022 | Migration | 1 | Device |
| 2022 | Material Deformation | 2 | Device |
| 2022 | Malposition of Device | 1 | Device |
| 2022 | Loss of Osseointegration | 52 | Device |
| 2022 | Fracture | 3 | Device |
| 2022 | Failure to Osseointegrate | 285 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 10 | Device |
| 2021 | Pain | 2 | Patient |
| 2021 | Failure of Implant | 8 | Patient |
| 2021 | Patient Device Interaction Problem | 2 | Device |
| 2021 | Osseointegration Problem | 2 | Device |
| 2021 | Failure to Osseointegrate | 22 | Device |
| 2021 | Adverse Event Without Identified Device or Use Problem | 2 | Device |
| 2020 | Failure of Implant | 2 | Patient |
| 2020 | Failure to Osseointegrate | 4 | Device |