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 | 22 | Patient |
2024 | Sinus Perforation | 4 | Patient |
2024 | Pain | 44 | Patient |
2024 | Osteomyelitis | 2 | Patient |
2024 | Numbness | 4 | Patient |
2024 | Implant Pain | 3 | Patient |
2024 | Foreign Body In Patient | 1 | Patient |
2024 | Failure of Implant | 420 | Patient |
2024 | Bone Fracture(s) | 4 | Patient |
2024 | Abscess | 8 | Patient |
2024 | Premature Separation | 4 | Device |
2024 | Osseointegration Problem | 4 | Device |
2024 | Migration | 1 | Device |
2024 | Malposition of Device | 4 | Device |
2024 | Loss of Osseointegration | 146 | Device |
2024 | Fracture | 4 | Device |
2024 | Failure to Osseointegrate | 157 | Device |
2024 | Device Markings/Labelling Problem | 9 | Device |
2024 | Adverse Event Without Identified Device or Use Problem | 10 | Device |
2024 | Activation, Positioning or Separation Problem | 1 | Device |
2023 | Unspecified Infection | 45 | Patient |
2023 | Pain | 77 | Patient |
2023 | Osteopenia/ Osteoporosis | 1 | Patient |
2023 | Numbness | 24 | Patient |
2023 | Insufficient Information | 1 | Patient |
2023 | Implant Pain | 1 | Patient |
2023 | Foreign Body In Patient | 3 | Patient |
2023 | Fistula | 3 | Patient |
2023 | Failure of Implant | 665 | Patient |
2023 | Bone Fracture(s) | 3 | Patient |
2023 | Separation Failure | 4 | Device |
2023 | Patient Device Interaction Problem | 18 | Device |
2023 | Osseointegration Problem | 23 | Device |
2023 | Migration | 3 | Device |
2023 | Mechanical Problem | 3 | Device |
2023 | Material Deformation | 2 | Device |
2023 | Malposition of Device | 1 | Device |
2023 | Loss of Osseointegration | 219 | Device |
2023 | Insufficient Information | 1 | Device |
2023 | Fracture | 16 | Device |
2023 | Failure to Osseointegrate | 355 | Device |
2023 | Difficult to Remove | 2 | Device |
2023 | Difficult to Insert | 1 | Device |
2023 | Adverse Event Without Identified Device or Use Problem | 10 | Device |
2022 | Unspecified Infection | 23 | Patient |
2022 | Pain | 35 | Patient |
2022 | Numbness | 7 | Patient |
2022 | Foreign Body In Patient | 1 | Patient |
2022 | Failure of Implant | 210 | Patient |
2022 | Separation Failure | 1 | Device |
2022 | Patient Device Interaction Problem | 2 | Device |
2022 | Osseointegration Problem | 51 | Device |
2022 | Migration | 1 | Device |
2022 | Malposition of Device | 2 | Device |
2022 | Loss of Osseointegration | 218 | Device |
2022 | Insufficient Information | 2 | Device |
2022 | Fracture | 16 | Device |
2022 | Failure to Osseointegrate | 339 | Device |
2022 | Device Damaged by Another Device | 2 | Device |
2022 | Adverse Event Without Identified Device or Use Problem | 22 | Device |
2021 | Pain | 2 | Patient |
2021 | Insufficient Information | 2 | Patient |
2021 | Failure of Implant | 37 | Patient |
2021 | Osseointegration Problem | 8 | Device |
2021 | Malposition of Device | 3 | Device |
2021 | Loss of Osseointegration | 32 | Device |
2021 | Fracture | 6 | Device |
2021 | Failure to Osseointegrate | 88 | Device |
2020 | Pain | 2 | Patient |
2020 | Failure of Implant | 14 | Patient |
2020 | Osseointegration Problem | 2 | Device |
2020 | Failure to Osseointegrate | 23 | Device |