ENDOSSEOUS DENTAL IMPLANT
This device is manufactured by NOBEL BIOCARE USA, UNKNOWN.
The following problems were reported about this device:
Year | Description | Events/year | Type |
---|---|---|---|
2024 | Unspecified Infection | 6 | Patient |
2024 | Pain | 4 | Patient |
2024 | Osteomyelitis | 2 | Patient |
2024 | Inflammation | 4 | Patient |
2024 | Implant Pain | 2 | Patient |
2024 | Foreign Body In Patient | 4 | Patient |
2024 | Failure of Implant | 239 | Patient |
2024 | Abscess | 2 | Patient |
2024 | Premature Separation | 1 | Device |
2024 | Osseointegration Problem | 6 | Device |
2024 | Migration | 4 | Device |
2024 | Mechanical Problem | 2 | Device |
2024 | Loss of Osseointegration | 81 | Device |
2024 | Failure to Osseointegrate | 113 | Device |
2024 | Adverse Event Without Identified Device or Use Problem | 6 | Device |
2023 | Unspecified Infection | 16 | Patient |
2023 | Pain | 18 | Patient |
2023 | Numbness | 2 | Patient |
2023 | Insufficient Information | 4 | Patient |
2023 | Inflammation | 2 | Patient |
2023 | Fistula | 2 | Patient |
2023 | Failure of Implant | 260 | Patient |
2023 | Abscess | 4 | Patient |
2023 | Patient Device Interaction Problem | 4 | Device |
2023 | Osseointegration Problem | 6 | Device |
2023 | Mechanical Problem | 2 | Device |
2023 | Loss of Osseointegration | 105 | Device |
2023 | Insufficient Information | 4 | Device |
2023 | Fracture | 4 | Device |
2023 | Failure to Osseointegrate | 102 | Device |
2023 | Difficult to Remove | 6 | Device |
2023 | Difficult to Insert | 4 | Device |
2023 | Adverse Event Without Identified Device or Use Problem | 6 | Device |
2022 | Unspecified Infection | 2 | Patient |
2022 | Pain | 8 | Patient |
2022 | Numbness | 2 | Patient |
2022 | Failure of Implant | 58 | Patient |
2022 | Abscess | 2 | Patient |
2022 | Separation Failure | 4 | Device |
2022 | Osseointegration Problem | 20 | Device |
2022 | Loss of Osseointegration | 83 | Device |
2022 | Insufficient Information | 2 | Device |
2022 | Fracture | 8 | Device |
2022 | Failure to Osseointegrate | 137 | Device |
2022 | Adverse Event Without Identified Device or Use Problem | 8 | Device |
2021 | Failure of Implant | 4 | Patient |
2021 | Osseointegration Problem | 4 | Device |
2021 | Loss of Osseointegration | 10 | Device |
2021 | Failure to Osseointegrate | 20 | Device |
2020 | Failure of Implant | 6 | Patient |
2020 | Failure to Osseointegrate | 8 | Device |