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 | 29 | Patient |
| 2024 | Pain | 24 | Patient |
| 2024 | Numbness | 7 | Patient |
| 2024 | Foreign Body In Patient | 2 | Patient |
| 2024 | Fistula | 2 | Patient |
| 2024 | Failure of Implant | 395 | Patient |
| 2024 | Abscess | 5 | Patient |
| 2024 | Premature Separation | 4 | Device |
| 2024 | Naturally Worn | 2 | Device |
| 2024 | Migration | 2 | Device |
| 2024 | Mechanical Problem | 2 | Device |
| 2024 | Material Deformation | 1 | Device |
| 2024 | Loss of Osseointegration | 65 | Device |
| 2024 | Fracture | 1 | Device |
| 2024 | Failure to Osseointegrate | 228 | Device |
| 2024 | Difficult to Insert | 1 | Device |
| 2024 | Adverse Event Without Identified Device or Use Problem | 7 | Device |
| 2024 | Activation, Positioning or Separation Problem | 1 | Device |
| 2023 | Unspecified Infection | 26 | Patient |
| 2023 | Swelling/ Edema | 1 | Patient |
| 2023 | Sinus Perforation | 1 | Patient |
| 2023 | Pain | 32 | Patient |
| 2023 | Numbness | 8 | Patient |
| 2023 | Insufficient Information | 1 | Patient |
| 2023 | Inflammation | 1 | Patient |
| 2023 | Fistula | 1 | Patient |
| 2023 | Failure of Implant | 554 | Patient |
| 2023 | Bone Fracture(s) | 2 | Patient |
| 2023 | Patient Device Interaction Problem | 5 | Device |
| 2023 | Osseointegration Problem | 7 | Device |
| 2023 | Mechanical Problem | 1 | Device |
| 2023 | Malposition of Device | 1 | Device |
| 2023 | Loss of Osseointegration | 96 | Device |
| 2023 | Insufficient Information | 1 | Device |
| 2023 | Fracture | 2 | Device |
| 2023 | Failure to Osseointegrate | 361 | Device |
| 2023 | Adverse Event Without Identified Device or Use Problem | 5 | Device |
| 2022 | Unspecified Infection | 11 | Patient |
| 2022 | Pain | 15 | Patient |
| 2022 | Numbness | 4 | Patient |
| 2022 | Failure of Implant | 122 | Patient |
| 2022 | Separation Failure | 1 | Device |
| 2022 | Patient Device Interaction Problem | 2 | Device |
| 2022 | Osseointegration Problem | 28 | Device |
| 2022 | Material Deformation | 1 | Device |
| 2022 | Loss of Osseointegration | 68 | Device |
| 2022 | Insufficient Information | 1 | Device |
| 2022 | Fracture | 3 | Device |
| 2022 | Failure to Osseointegrate | 272 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 6 | Device |
| 2021 | Foreign Body In Patient | 2 | Patient |
| 2021 | Failure of Implant | 33 | Patient |
| 2021 | Migration | 2 | Device |
| 2021 | Loss of Osseointegration | 7 | Device |
| 2021 | Insufficient Information | 1 | Device |
| 2021 | Failure to Osseointegrate | 63 | Device |
| 2021 | Adverse Event Without Identified Device or Use Problem | 1 | Device |
| 2020 | Unspecified Infection | 2 | Patient |
| 2020 | Failure of Implant | 22 | Patient |
| 2020 | Material Deformation | 2 | Device |
| 2020 | Loss of Osseointegration | 6 | Device |
| 2020 | Failure to Osseointegrate | 25 | Device |