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 | 13 | Patient |
| 2024 | Sinus Perforation | 2 | Patient |
| 2024 | Pain | 16 | Patient |
| 2024 | Numbness | 10 | Patient |
| 2024 | Inflammation | 2 | Patient |
| 2024 | Implant Pain | 2 | Patient |
| 2024 | Hypersensitivity/Allergic reaction | 4 | Patient |
| 2024 | Foreign Body In Patient | 4 | Patient |
| 2024 | Failure of Implant | 438 | Patient |
| 2024 | Abscess | 4 | Patient |
| 2024 | Premature Separation | 4 | Device |
| 2024 | Osseointegration Problem | 2 | Device |
| 2024 | Migration | 4 | Device |
| 2024 | Loss of Osseointegration | 113 | Device |
| 2024 | Fracture | 11 | Device |
| 2024 | Flaked | 2 | Device |
| 2024 | Failure to Osseointegrate | 234 | Device |
| 2024 | Difficult to Remove | 2 | Device |
| 2024 | Device Markings/Labelling Problem | 2 | Device |
| 2024 | Activation, Positioning or Separation Problem | 1 | Device |
| 2023 | Unspecified Infection | 38 | Patient |
| 2023 | Pain | 42 | Patient |
| 2023 | Numbness | 14 | Patient |
| 2023 | Insufficient Information | 4 | Patient |
| 2023 | Foreign Body In Patient | 8 | Patient |
| 2023 | Failure of Implant | 531 | Patient |
| 2023 | Bone Fracture(s) | 4 | Patient |
| 2023 | Premature Separation | 4 | Device |
| 2023 | Patient Device Interaction Problem | 20 | Device |
| 2023 | Osseointegration Problem | 24 | Device |
| 2023 | Migration | 4 | Device |
| 2023 | Loss of Osseointegration | 124 | Device |
| 2023 | Insufficient Information | 4 | Device |
| 2023 | Fracture | 12 | Device |
| 2023 | Failure to Osseointegrate | 326 | Device |
| 2023 | Difficult to Insert | 4 | Device |
| 2023 | Device Markings/Labelling Problem | 4 | Device |
| 2023 | Adverse Event Without Identified Device or Use Problem | 2 | Device |
| 2022 | Unspecified Infection | 6 | Patient |
| 2022 | Sinus Perforation | 2 | Patient |
| 2022 | Pain | 25 | Patient |
| 2022 | Numbness | 4 | Patient |
| 2022 | Failure of Implant | 223 | Patient |
| 2022 | Patient Device Interaction Problem | 2 | Device |
| 2022 | Osseointegration Problem | 44 | Device |
| 2022 | Material Deformation | 2 | Device |
| 2022 | Malposition of Device | 2 | Device |
| 2022 | Loss of Osseointegration | 99 | Device |
| 2022 | Insufficient Information | 2 | Device |
| 2022 | Fracture | 4 | Device |
| 2022 | Failure to Osseointegrate | 340 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 14 | Device |
| 2021 | Numbness | 2 | Patient |
| 2021 | Fistula | 2 | Patient |
| 2021 | Failure of Implant | 31 | Patient |
| 2021 | Osseointegration Problem | 2 | Device |
| 2021 | Loss of Osseointegration | 8 | Device |
| 2021 | Failure to Osseointegrate | 67 | Device |
| 2021 | Device Markings/Labelling Problem | 2 | Device |
| 2021 | Adverse Event Without Identified Device or Use Problem | 2 | Device |
| 2021 | Activation, Positioning or Separation Problem | 2 | Device |
| 2020 | Failure of Implant | 14 | Patient |
| 2020 | Osseointegration Problem | 4 | Device |
| 2020 | Loss of Osseointegration | 2 | Device |
| 2020 | Fracture | 2 | Device |
| 2020 | Failure to Osseointegrate | 24 | Device |