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 | 2 | Patient |
2024 | Pain | 1 | Patient |
2024 | Fistula | 2 | Patient |
2024 | Failure of Implant | 90 | Patient |
2024 | Loss of Osseointegration | 38 | Device |
2024 | Fracture | 2 | Device |
2024 | Failure to Osseointegrate | 36 | Device |
2024 | Adverse Event Without Identified Device or Use Problem | 2 | Device |
2023 | Unspecified Infection | 8 | Patient |
2023 | Sinus Perforation | 1 | Patient |
2023 | Pain | 12 | Patient |
2023 | Numbness | 4 | Patient |
2023 | Foreign Body In Patient | 2 | Patient |
2023 | Fistula | 1 | Patient |
2023 | Failure of Implant | 179 | Patient |
2023 | Bone Fracture(s) | 1 | Patient |
2023 | Patient Device Interaction Problem | 11 | Device |
2023 | Osseointegration Problem | 10 | Device |
2023 | Migration | 2 | Device |
2023 | Malposition of Device | 1 | Device |
2023 | Loss of Osseointegration | 60 | Device |
2023 | Fracture | 4 | Device |
2023 | Failure to Osseointegrate | 92 | Device |
2023 | Difficult to Insert | 2 | Device |
2023 | Device Markings/Labelling Problem | 1 | Device |
2023 | Adverse Event Without Identified Device or Use Problem | 2 | Device |
2022 | Unspecified Infection | 8 | Patient |
2022 | Pain | 4 | Patient |
2022 | Failure of Implant | 89 | Patient |
2022 | Separation Failure | 2 | Device |
2022 | Patient Device Interaction Problem | 2 | Device |
2022 | Osseointegration Problem | 20 | Device |
2022 | Malposition of Device | 1 | Device |
2022 | Loss of Osseointegration | 85 | Device |
2022 | Fracture | 10 | Device |
2022 | Failure to Osseointegrate | 143 | Device |
2022 | Adverse Event Without Identified Device or Use Problem | 6 | Device |
2021 | Unspecified Infection | 2 | Patient |
2021 | Failure of Implant | 21 | Patient |
2021 | Osseointegration Problem | 4 | Device |
2021 | Loss of Osseointegration | 10 | Device |
2021 | Insufficient Information | 1 | Device |
2021 | Failure to Osseointegrate | 34 | Device |
2020 | Unspecified Infection | 2 | Patient |
2020 | Failure of Implant | 4 | Patient |
2020 | Patient Device Interaction Problem | 1 | Device |
2020 | Loss of Osseointegration | 4 | Device |
2020 | Failure to Osseointegrate | 2 | Device |
2019 | Failure of Implant | 2 | Patient |
2019 | Osseointegration Problem | 18 | Device |
2019 | Loss of Osseointegration | 77 | Device |
2019 | Fracture | 8 | Device |
2019 | Failure to Osseointegrate | 133 | Device |
2019 | Adverse Event Without Identified Device or Use Problem | 8 | Device |
2018 | Osseointegration Problem | 2 | Device |
2018 | Loss of Osseointegration | 10 | Device |
2018 | Fracture | 2 | Device |
2018 | Failure to Osseointegrate | 16 | Device |
2017 | Loss of Osseointegration | 2 | Device |
2013 | Failure of Implant | 2 | Patient |
2013 | Loss of Osseointegration | 2 | Device |
2009 | Loss of Osseointegration | 2 | Device |