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 | 18 | Patient |
| 2024 | Sinus Perforation | 2 | Patient |
| 2024 | Pain | 12 | Patient |
| 2024 | Osteomyelitis | 4 | Patient |
| 2024 | Numbness | 8 | Patient |
| 2024 | Inflammation | 4 | Patient |
| 2024 | Implant Pain | 2 | Patient |
| 2024 | Hypersensitivity/Allergic reaction | 2 | Patient |
| 2024 | Foreign Body In Patient | 2 | Patient |
| 2024 | Fistula | 2 | Patient |
| 2024 | Failure of Implant | 536 | Patient |
| 2024 | Bone Fracture(s) | 4 | Patient |
| 2024 | Abscess | 10 | Patient |
| 2024 | Premature Separation | 12 | Device |
| 2024 | Osseointegration Problem | 2 | Device |
| 2024 | Migration | 2 | Device |
| 2024 | Mechanical Problem | 2 | Device |
| 2024 | Material Discolored | 2 | Device |
| 2024 | Loss of Osseointegration | 45 | Device |
| 2024 | Fracture | 2 | Device |
| 2024 | Flaked | 2 | Device |
| 2024 | Failure to Osseointegrate | 318 | Device |
| 2024 | Difficult to Insert | 6 | Device |
| 2024 | Device Markings/Labelling Problem | 4 | Device |
| 2024 | Adverse Event Without Identified Device or Use Problem | 10 | Device |
| 2024 | Activation, Positioning or Separation Problem | 2 | Device |
| 2023 | Unspecified Infection | 30 | Patient |
| 2023 | Sinus Perforation | 4 | Patient |
| 2023 | Pain | 86 | Patient |
| 2023 | Numbness | 12 | Patient |
| 2023 | Insufficient Information | 6 | Patient |
| 2023 | Inflammation | 4 | Patient |
| 2023 | Foreign Body In Patient | 2 | Patient |
| 2023 | Fistula | 2 | Patient |
| 2023 | Failure of Implant | 690 | Patient |
| 2023 | Bone Fracture(s) | 4 | Patient |
| 2023 | Abscess | 6 | Patient |
| 2023 | Separation Failure | 4 | Device |
| 2023 | Premature Separation | 6 | Device |
| 2023 | Patient Device Interaction Problem | 45 | Device |
| 2023 | Osseointegration Problem | 22 | Device |
| 2023 | Migration | 4 | Device |
| 2023 | Mechanical Problem | 6 | Device |
| 2023 | Malposition of Device | 6 | Device |
| 2023 | Loss of Osseointegration | 60 | Device |
| 2023 | Insufficient Information | 6 | Device |
| 2023 | Fracture | 4 | Device |
| 2023 | Failure to Osseointegrate | 530 | Device |
| 2023 | Difficult to Insert | 4 | Device |
| 2023 | Device Markings/Labelling Problem | 10 | Device |
| 2023 | Adverse Event Without Identified Device or Use Problem | 12 | Device |
| 2023 | Activation, Positioning or Separation Problem | 2 | Device |
| 2022 | Unspecified Infection | 18 | Patient |
| 2022 | Pain | 32 | Patient |
| 2022 | Numbness | 4 | Patient |
| 2022 | Failure of Implant | 101 | Patient |
| 2022 | Osseointegration Problem | 45 | Device |
| 2022 | Malposition of Device | 4 | Device |
| 2022 | Loss of Osseointegration | 50 | Device |
| 2022 | Insufficient Information | 2 | Device |
| 2022 | Fracture | 8 | Device |
| 2022 | Failure to Osseointegrate | 431 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 22 | Device |
| 2021 | Unspecified Infection | 2 | Patient |
| 2021 | Pain | 1 | Patient |
| 2021 | Failure of Implant | 11 | Patient |
| 2021 | Osseointegration Problem | 2 | Device |
| 2021 | Loss of Osseointegration | 4 | Device |
| 2021 | Failure to Osseointegrate | 27 | Device |
| 2020 | Failure of Implant | 6 | Patient |
| 2020 | Loss of Osseointegration | 2 | Device |
| 2020 | Failure to Osseointegrate | 4 | Device |