ENDOSSEOUS DENTAL IMPLANT
This device is manufactured by BOSTON SCIENTIFIC CORPORATION, NOBEL BIOCARE USA.
The following problems were reported about this device:
| Year | Description | Events/year | Type |
|---|---|---|---|
| 2024 | Unspecified Infection | 38 | Patient |
| 2024 | Pain | 27 | Patient |
| 2024 | Numbness | 8 | Patient |
| 2024 | Foreign Body In Patient | 4 | Patient |
| 2024 | Fistula | 2 | Patient |
| 2024 | Failure of Implant | 516 | Patient |
| 2024 | Abscess | 2 | Patient |
| 2024 | Migration | 4 | Device |
| 2024 | Loss of Osseointegration | 68 | Device |
| 2024 | Fracture | 4 | Device |
| 2024 | Failure to Osseointegrate | 346 | Device |
| 2024 | Adverse Event Without Identified Device or Use Problem | 6 | Device |
| 2023 | Unspecified Infection | 26 | Patient |
| 2023 | Pain | 39 | Patient |
| 2023 | Numbness | 18 | Patient |
| 2023 | Foreign Body In Patient | 2 | Patient |
| 2023 | Fistula | 1 | Patient |
| 2023 | Failure of Implant | 719 | Patient |
| 2023 | Bone Fracture(s) | 2 | Patient |
| 2023 | Abscess | 8 | Patient |
| 2023 | Patient Device Interaction Problem | 12 | Device |
| 2023 | Osseointegration Problem | 12 | Device |
| 2023 | Migration | 5 | Device |
| 2023 | Malposition of Device | 1 | Device |
| 2023 | Loss of Osseointegration | 86 | Device |
| 2023 | Fracture | 4 | Device |
| 2023 | Failure to Osseointegrate | 528 | Device |
| 2023 | Difficult to Remove | 2 | Device |
| 2023 | Difficult to Insert | 2 | Device |
| 2023 | Device Damaged by Another Device | 1 | Device |
| 2023 | Adverse Event Without Identified Device or Use Problem | 17 | Device |
| 2022 | Unspecified Infection | 15 | Patient |
| 2022 | Pain | 19 | Patient |
| 2022 | Numbness | 2 | Patient |
| 2022 | Failure of Implant | 201 | Patient |
| 2022 | Bone Fracture(s) | 4 | Patient |
| 2022 | Osseointegration Problem | 29 | Device |
| 2022 | Malposition of Device | 4 | Device |
| 2022 | Loss of Osseointegration | 78 | Device |
| 2022 | Insufficient Information | 1 | Device |
| 2022 | Fracture | 16 | Device |
| 2022 | Failure to Osseointegrate | 461 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 13 | Device |
| 2021 | Failure of Implant | 15 | Patient |
| 2021 | Osseointegration Problem | 2 | Device |
| 2021 | Malposition of Device | 2 | Device |
| 2021 | Loss of Osseointegration | 7 | Device |
| 2021 | Insufficient Information | 1 | Device |
| 2021 | Failure to Osseointegrate | 76 | Device |
| 2021 | Adverse Event Without Identified Device or Use Problem | 2 | Device |
| 2020 | Pain | 2 | Patient |
| 2020 | Failure of Implant | 20 | Patient |
| 2020 | Loss of Osseointegration | 9 | Device |
| 2020 | Insufficient Information | 1 | Device |
| 2020 | Failure to Osseointegrate | 24 | Device |