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 | 2 | Patient |
2024 | Foreign Body In Patient | 2 | Patient |
2024 | Failure of Implant | 69 | Patient |
2024 | Bone Fracture(s) | 2 | Patient |
2024 | Abscess | 6 | Patient |
2024 | Migration | 2 | Device |
2024 | Loss of Osseointegration | 4 | Device |
2024 | Fracture | 2 | Device |
2024 | Failure to Osseointegrate | 33 | Device |
2024 | Adverse Event Without Identified Device or Use Problem | 2 | Device |
2024 | Activation, Positioning or Separation Problem | 2 | Device |
2023 | Unspecified Infection | 10 | Patient |
2023 | Pain | 10 | Patient |
2023 | Insufficient Information | 2 | Patient |
2023 | Inflammation | 2 | Patient |
2023 | Failure of Implant | 164 | Patient |
2023 | Bone Fracture(s) | 2 | Patient |
2023 | Patient Device Interaction Problem | 14 | Device |
2023 | Osseointegration Problem | 12 | Device |
2023 | Manufacturing, Packaging or Shipping Problem | 2 | Device |
2023 | Loss of Osseointegration | 18 | Device |
2023 | Failure to Osseointegrate | 101 | Device |
2023 | Adverse Event Without Identified Device or Use Problem | 8 | Device |
2022 | Unspecified Infection | 2 | Patient |
2022 | Pain | 2 | Patient |
2022 | Failure of Implant | 38 | Patient |
2022 | Osseointegration Problem | 12 | Device |
2022 | Material Deformation | 2 | Device |
2022 | Loss of Osseointegration | 22 | Device |
2022 | Insufficient Information | 4 | Device |
2022 | Fracture | 2 | Device |
2022 | Failure to Osseointegrate | 126 | Device |
2022 | Device Damaged by Another Device | 2 | Device |
2022 | Adverse Event Without Identified Device or Use Problem | 14 | Device |
2021 | Failure of Implant | 2 | Patient |
2021 | Failure to Osseointegrate | 12 | Device |
2020 | Failure of Implant | 2 | Patient |
2019 | Loss of Osseointegration | 30 | Device |
2019 | Failure to Osseointegrate | 85 | Device |
2019 | Adverse Event Without Identified Device or Use Problem | 4 | Device |
2018 | Failure to Osseointegrate | 6 | Device |
2015 | Failure to Osseointegrate | 4 | Device |