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 | 42 | Patient |
| 2024 | Pain | 46 | Patient |
| 2024 | Osteomyelitis | 2 | Patient |
| 2024 | Numbness | 4 | Patient |
| 2024 | Inflammation | 12 | Patient |
| 2024 | Foreign Body In Patient | 8 | Patient |
| 2024 | Fistula | 16 | Patient |
| 2024 | Failure of Implant | 1328 | Patient |
| 2024 | Bone Fracture(s) | 4 | Patient |
| 2024 | Abscess | 22 | Patient |
| 2024 | Premature Separation | 12 | Device |
| 2024 | Osseointegration Problem | 14 | Device |
| 2024 | Migration | 6 | Device |
| 2024 | Mechanical Problem | 2 | Device |
| 2024 | Loss of Osseointegration | 302 | Device |
| 2024 | Fracture | 21 | Device |
| 2024 | Failure to Osseointegrate | 747 | Device |
| 2024 | Difficult to Insert | 5 | Device |
| 2024 | Device Markings/Labelling Problem | 4 | Device |
| 2024 | Device Damaged by Another Device | 1 | Device |
| 2024 | Adverse Event Without Identified Device or Use Problem | 40 | Device |
| 2024 | Activation, Positioning or Separation Problem | 2 | Device |
| 2023 | Unspecified Infection | 61 | Patient |
| 2023 | Sinus Perforation | 4 | Patient |
| 2023 | Paresthesia | 2 | Patient |
| 2023 | Pain | 95 | Patient |
| 2023 | Numbness | 14 | Patient |
| 2023 | Insufficient Information | 9 | Patient |
| 2023 | Foreign Body In Patient | 4 | Patient |
| 2023 | Fistula | 12 | Patient |
| 2023 | Failure of Implant | 1091 | Patient |
| 2023 | Bone Fracture(s) | 2 | Patient |
| 2023 | Abscess | 11 | Patient |
| 2023 | Premature Separation | 2 | Device |
| 2023 | Patient Device Interaction Problem | 27 | Device |
| 2023 | Osseointegration Problem | 65 | Device |
| 2023 | Migration | 5 | Device |
| 2023 | Mechanical Problem | 10 | Device |
| 2023 | Malposition of Device | 1 | Device |
| 2023 | Loss of Osseointegration | 247 | Device |
| 2023 | Insufficient Information | 7 | Device |
| 2023 | Fracture | 21 | Device |
| 2023 | Failure to Osseointegrate | 665 | Device |
| 2023 | Difficult to Insert | 2 | Device |
| 2023 | Adverse Event Without Identified Device or Use Problem | 22 | Device |
| 2023 | Activation, Positioning or Separation Problem | 3 | Device |
| 2022 | Unspecified Infection | 29 | Patient |
| 2022 | Pain | 44 | Patient |
| 2022 | Numbness | 4 | Patient |
| 2022 | Failure of Implant | 314 | Patient |
| 2022 | Bone Fracture(s) | 2 | Patient |
| 2022 | Patient Device Interaction Problem | 1 | Device |
| 2022 | Osseointegration Problem | 131 | Device |
| 2022 | Material Deformation | 4 | Device |
| 2022 | Malposition of Device | 2 | Device |
| 2022 | Loss of Osseointegration | 231 | Device |
| 2022 | Insufficient Information | 11 | Device |
| 2022 | Fracture | 39 | Device |
| 2022 | Failure to Osseointegrate | 592 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 45 | Device |
| 2021 | Unspecified Infection | 2 | Patient |
| 2021 | Pain | 3 | Patient |
| 2021 | Failure of Implant | 44 | Patient |
| 2021 | Patient Device Interaction Problem | 1 | Device |
| 2021 | Osseointegration Problem | 14 | Device |
| 2021 | Loss of Osseointegration | 36 | Device |
| 2021 | Fracture | 4 | Device |
| 2021 | Failure to Osseointegrate | 101 | Device |
| 2021 | Adverse Event Without Identified Device or Use Problem | 3 | Device |
| 2020 | Unspecified Infection | 4 | Patient |
| 2020 | Pain | 2 | Patient |
| 2020 | Numbness | 2 | Patient |
| 2020 | Insufficient Information | 1 | Patient |
| 2020 | Failure of Implant | 14 | Patient |
| 2020 | Loss of Osseointegration | 12 | Device |
| 2020 | Insufficient Information | 1 | Device |
| 2020 | Failure to Osseointegrate | 18 | Device |