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 | 16 | Patient |
| 2024 | Sinus Perforation | 2 | Patient |
| 2024 | Pain | 2 | Patient |
| 2024 | Numbness | 2 | Patient |
| 2024 | Inflammation | 2 | Patient |
| 2024 | Implant Pain | 2 | Patient |
| 2024 | Foreign Body In Patient | 6 | Patient |
| 2024 | Fistula | 2 | Patient |
| 2024 | Failure of Implant | 320 | Patient |
| 2024 | Bone Fracture(s) | 2 | Patient |
| 2024 | Abscess | 1 | Patient |
| 2024 | Premature Separation | 3 | Device |
| 2024 | Osseointegration Problem | 2 | Device |
| 2024 | Migration | 4 | Device |
| 2024 | Material Discolored | 2 | Device |
| 2024 | Loss of Osseointegration | 38 | Device |
| 2024 | Fracture | 8 | Device |
| 2024 | Failure to Osseointegrate | 190 | Device |
| 2024 | Difficult to Remove | 1 | Device |
| 2024 | Device Markings/Labelling Problem | 1 | Device |
| 2024 | Adverse Event Without Identified Device or Use Problem | 6 | Device |
| 2024 | Activation, Positioning or Separation Problem | 2 | Device |
| 2023 | Unspecified Infection | 16 | Patient |
| 2023 | Pain | 38 | Patient |
| 2023 | Numbness | 11 | Patient |
| 2023 | Insufficient Information | 4 | Patient |
| 2023 | Foreign Body In Patient | 5 | Patient |
| 2023 | Fistula | 2 | Patient |
| 2023 | Failure of Implant | 463 | Patient |
| 2023 | Bone Fracture(s) | 7 | Patient |
| 2023 | Abscess | 6 | Patient |
| 2023 | Premature Separation | 3 | Device |
| 2023 | Patient Device Interaction Problem | 30 | Device |
| 2023 | Osseointegration Problem | 16 | Device |
| 2023 | Migration | 6 | Device |
| 2023 | Mechanical Problem | 2 | Device |
| 2023 | Material Deformation | 2 | Device |
| 2023 | Loss of Osseointegration | 51 | Device |
| 2023 | Insufficient Information | 4 | Device |
| 2023 | Fracture | 10 | Device |
| 2023 | Failure to Osseointegrate | 325 | Device |
| 2023 | Device Markings/Labelling Problem | 4 | Device |
| 2023 | Adverse Event Without Identified Device or Use Problem | 17 | Device |
| 2023 | Activation, Positioning or Separation Problem | 1 | Device |
| 2022 | Unspecified Infection | 9 | Patient |
| 2022 | Pain | 9 | Patient |
| 2022 | Numbness | 2 | Patient |
| 2022 | Failure of Implant | 82 | Patient |
| 2022 | Separation Failure | 2 | Device |
| 2022 | Osseointegration Problem | 31 | Device |
| 2022 | Malposition of Device | 2 | Device |
| 2022 | Loss of Osseointegration | 16 | Device |
| 2022 | Fracture | 5 | Device |
| 2022 | Failure to Osseointegrate | 280 | Device |
| 2022 | Defective Device | 1 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 12 | Device |
| 2021 | Numbness | 2 | Patient |
| 2021 | Failure of Implant | 4 | Patient |
| 2021 | Osseointegration Problem | 6 | Device |
| 2021 | Fracture | 2 | Device |
| 2021 | Failure to Osseointegrate | 16 | Device |