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 | 17 | Patient |
| 2024 | Pain | 21 | Patient |
| 2024 | Osteomyelitis | 1 | Patient |
| 2024 | Numbness | 6 | Patient |
| 2024 | Failure of Implant | 401 | Patient |
| 2024 | Abscess | 3 | Patient |
| 2024 | Premature Separation | 4 | Device |
| 2024 | Osseointegration Problem | 4 | Device |
| 2024 | Mechanical Problem | 1 | Device |
| 2024 | Loss of Osseointegration | 59 | Device |
| 2024 | Fracture | 1 | Device |
| 2024 | Failure to Osseointegrate | 242 | Device |
| 2024 | Difficult to Insert | 2 | Device |
| 2024 | Adverse Event Without Identified Device or Use Problem | 3 | Device |
| 2024 | Activation, Positioning or Separation Problem | 2 | Device |
| 2023 | Unspecified Infection | 18 | Patient |
| 2023 | Pain | 23 | Patient |
| 2023 | Osteomyelitis | 2 | Patient |
| 2023 | Numbness | 3 | Patient |
| 2023 | Insufficient Information | 2 | Patient |
| 2023 | Inflammation | 1 | Patient |
| 2023 | Foreign Body In Patient | 2 | Patient |
| 2023 | Failure of Implant | 584 | Patient |
| 2023 | Bone Fracture(s) | 2 | Patient |
| 2023 | Abscess | 2 | Patient |
| 2023 | Premature Separation | 1 | Device |
| 2023 | Patient Device Interaction Problem | 12 | Device |
| 2023 | Osseointegration Problem | 9 | Device |
| 2023 | Migration | 3 | Device |
| 2023 | Mechanical Problem | 3 | Device |
| 2023 | Malposition of Device | 1 | Device |
| 2023 | Loss of Osseointegration | 149 | Device |
| 2023 | Insufficient Information | 2 | Device |
| 2023 | Failure to Osseointegrate | 358 | Device |
| 2023 | Difficult to Remove | 1 | Device |
| 2023 | Difficult to Insert | 1 | Device |
| 2023 | Device Markings/Labelling Problem | 1 | Device |
| 2023 | Adverse Event Without Identified Device or Use Problem | 10 | Device |
| 2023 | Activation, Positioning or Separation Problem | 1 | Device |
| 2022 | Unspecified Infection | 10 | Patient |
| 2022 | Sinus Perforation | 1 | Patient |
| 2022 | Pain | 8 | Patient |
| 2022 | Numbness | 2 | Patient |
| 2022 | Inflammation | 1 | Patient |
| 2022 | Failure of Implant | 183 | Patient |
| 2022 | Osseointegration Problem | 22 | Device |
| 2022 | Material Deformation | 2 | Device |
| 2022 | Loss of Osseointegration | 91 | Device |
| 2022 | Fracture | 2 | Device |
| 2022 | Failure to Osseointegrate | 293 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 15 | Device |
| 2021 | Unspecified Infection | 7 | Patient |
| 2021 | Pain | 10 | Patient |
| 2021 | Numbness | 2 | Patient |
| 2021 | Failure of Implant | 33 | Patient |
| 2021 | Osseointegration Problem | 3 | Device |
| 2021 | Loss of Osseointegration | 5 | Device |
| 2021 | Insufficient Information | 2 | Device |
| 2021 | Failure to Osseointegrate | 60 | Device |
| 2020 | Pain | 2 | Patient |
| 2020 | Failure of Implant | 10 | Patient |
| 2020 | Loss of Osseointegration | 2 | Device |
| 2020 | Failure to Osseointegrate | 7 | Device |