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 | 5 | Patient |
| 2024 | Pain | 20 | Patient |
| 2024 | Osteomyelitis | 2 | Patient |
| 2024 | Numbness | 2 | Patient |
| 2024 | Fistula | 4 | Patient |
| 2024 | Failure of Implant | 133 | Patient |
| 2024 | Abscess | 1 | Patient |
| 2024 | Loss of Osseointegration | 65 | Device |
| 2024 | Failure to Osseointegrate | 42 | Device |
| 2024 | Adverse Event Without Identified Device or Use Problem | 7 | Device |
| 2023 | Unspecified Infection | 3 | Patient |
| 2023 | Sinus Perforation | 2 | Patient |
| 2023 | Pain | 13 | Patient |
| 2023 | Numbness | 2 | Patient |
| 2023 | Inflammation | 2 | Patient |
| 2023 | Failure of Implant | 189 | Patient |
| 2023 | Abscess | 2 | Patient |
| 2023 | Osseointegration Problem | 5 | Device |
| 2023 | Malposition of Device | 2 | Device |
| 2023 | Loss of Osseointegration | 94 | Device |
| 2023 | Fracture | 2 | Device |
| 2023 | Failure to Osseointegrate | 69 | Device |
| 2023 | Difficult to Insert | 1 | Device |
| 2023 | Adverse Event Without Identified Device or Use Problem | 1 | Device |
| 2022 | Unspecified Infection | 1 | Patient |
| 2022 | Pain | 3 | Patient |
| 2022 | Numbness | 4 | Patient |
| 2022 | Failure of Implant | 54 | Patient |
| 2022 | Osseointegration Problem | 6 | Device |
| 2022 | Loss of Osseointegration | 104 | Device |
| 2022 | Failure to Osseointegrate | 86 | Device |
| 2021 | Pain | 4 | Patient |
| 2021 | Failure of Implant | 15 | Patient |
| 2021 | Loss of Osseointegration | 20 | Device |
| 2021 | Failure to Osseointegrate | 17 | Device |
| 2020 | Failure to Osseointegrate | 6 | Device |
| 2019 | Failure of Implant | 3 | Patient |
| 2019 | Osseointegration Problem | 4 | Device |
| 2019 | Mechanical Problem | 1 | Device |
| 2019 | Loss of Osseointegration | 85 | Device |
| 2019 | Fracture | 3 | Device |
| 2019 | Failure to Osseointegrate | 80 | Device |
| 2019 | Adverse Event Without Identified Device or Use Problem | 1 | Device |
| 2018 | Loss of Osseointegration | 35 | Device |
| 2018 | Failure to Osseointegrate | 64 | Device |
| 2017 | Failure of Implant | 4 | Patient |
| 2017 | Loss of Osseointegration | 3 | Device |
| 2017 | Failure to Osseointegrate | 3 | Device |
| 2016 | Failure of Implant | 2 | Patient |
| 2016 | Loss of Osseointegration | 2 | Device |
| 2016 | Failure to Osseointegrate | 3 | Device |
| 2015 | Failure of Implant | 2 | Patient |
| 2015 | Loss of Osseointegration | 1 | Device |
| 2015 | Failure to Osseointegrate | 2 | Device |
| 2014 | Loss of Osseointegration | 1 | Device |
| 2010 | Failure to Osseointegrate | 1 | Device |