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 | 34 | Patient |
| 2024 | Sinus Perforation | 4 | Patient |
| 2024 | Pain | 11 | Patient |
| 2024 | Osteomyelitis | 4 | Patient |
| 2024 | Insufficient Information | 2 | Patient |
| 2024 | Inflammation | 12 | Patient |
| 2024 | Foreign Body In Patient | 10 | Patient |
| 2024 | Fistula | 2 | Patient |
| 2024 | Failure of Implant | 784 | Patient |
| 2024 | Bone Fracture(s) | 5 | Patient |
| 2024 | Abscess | 15 | Patient |
| 2024 | Premature Separation | 2 | Device |
| 2024 | Osseointegration Problem | 8 | Device |
| 2024 | Migration | 13 | Device |
| 2024 | Mechanical Problem | 2 | Device |
| 2024 | Material Discolored | 2 | Device |
| 2024 | Malposition of Device | 2 | Device |
| 2024 | Loss of Osseointegration | 112 | Device |
| 2024 | Insufficient Information | 2 | Device |
| 2024 | Fracture | 12 | Device |
| 2024 | Failure to Osseointegrate | 489 | Device |
| 2024 | Difficult to Insert | 11 | Device |
| 2024 | Device Markings/Labelling Problem | 5 | Device |
| 2024 | Adverse Event Without Identified Device or Use Problem | 6 | Device |
| 2024 | Activation, Positioning or Separation Problem | 9 | Device |
| 2023 | Unspecified Infection | 24 | Patient |
| 2023 | Sinus Perforation | 2 | Patient |
| 2023 | Pain | 87 | Patient |
| 2023 | Numbness | 9 | Patient |
| 2023 | Nerve Damage | 2 | Patient |
| 2023 | Insufficient Information | 8 | Patient |
| 2023 | Implant Pain | 2 | Patient |
| 2023 | Foreign Body In Patient | 5 | Patient |
| 2023 | Fistula | 4 | Patient |
| 2023 | Failure of Implant | 589 | Patient |
| 2023 | Bone Fracture(s) | 2 | Patient |
| 2023 | Abscess | 11 | Patient |
| 2023 | Separation Failure | 2 | Device |
| 2023 | Premature Separation | 2 | Device |
| 2023 | Patient Device Interaction Problem | 32 | Device |
| 2023 | Osseointegration Problem | 30 | Device |
| 2023 | Migration | 5 | Device |
| 2023 | Mechanical Problem | 4 | Device |
| 2023 | Material Deformation | 2 | Device |
| 2023 | Loss of Osseointegration | 75 | Device |
| 2023 | Insufficient Information | 7 | Device |
| 2023 | Fracture | 16 | Device |
| 2023 | Failure to Osseointegrate | 391 | Device |
| 2023 | Difficult to Insert | 4 | Device |
| 2023 | Device Markings/Labelling Problem | 4 | Device |
| 2023 | Adverse Event Without Identified Device or Use Problem | 21 | Device |
| 2023 | Activation, Positioning or Separation Problem | 5 | Device |
| 2022 | Unspecified Infection | 9 | Patient |
| 2022 | Pain | 28 | Patient |
| 2022 | Numbness | 2 | Patient |
| 2022 | Foreign Body In Patient | 4 | Patient |
| 2022 | Failure of Implant | 111 | Patient |
| 2022 | Abscess | 2 | Patient |
| 2022 | Separation Failure | 2 | Device |
| 2022 | Patient Device Interaction Problem | 8 | Device |
| 2022 | Osseointegration Problem | 55 | Device |
| 2022 | Migration | 4 | Device |
| 2022 | Material Deformation | 2 | Device |
| 2022 | Malposition of Device | 6 | Device |
| 2022 | Loss of Osseointegration | 26 | Device |
| 2022 | Fracture | 4 | Device |
| 2022 | Failure to Osseointegrate | 350 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 30 | Device |
| 2021 | Unspecified Infection | 2 | Patient |
| 2021 | Failure of Implant | 6 | Patient |
| 2021 | Separation Failure | 2 | Device |
| 2021 | Loss of Osseointegration | 2 | Device |
| 2021 | Failure to Osseointegrate | 24 | Device |
| 2021 | Adverse Event Without Identified Device or Use Problem | 2 | Device |
| 2020 | Failure of Implant | 6 | Patient |
| 2020 | Failure to Osseointegrate | 6 | Device |