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 | 2 | Patient |
| 2024 | Pain | 14 | Patient |
| 2024 | Numbness | 7 | Patient |
| 2024 | Fistula | 2 | Patient |
| 2024 | Failure of Implant | 309 | Patient |
| 2024 | Bone Fracture(s) | 2 | Patient |
| 2024 | Abscess | 16 | Patient |
| 2024 | Premature Separation | 2 | Device |
| 2024 | Osseointegration Problem | 2 | Device |
| 2024 | Naturally Worn | 2 | Device |
| 2024 | Mechanical Problem | 2 | Device |
| 2024 | Loss of Osseointegration | 24 | Device |
| 2024 | Fracture | 6 | Device |
| 2024 | Failure to Osseointegrate | 177 | Device |
| 2024 | Device Markings/Labelling Problem | 5 | Device |
| 2024 | Adverse Event Without Identified Device or Use Problem | 13 | Device |
| 2024 | Activation, Positioning or Separation Problem | 3 | Device |
| 2023 | Unspecified Infection | 14 | Patient |
| 2023 | Pain | 39 | Patient |
| 2023 | Numbness | 4 | Patient |
| 2023 | Insufficient Information | 9 | Patient |
| 2023 | Foreign Body In Patient | 2 | Patient |
| 2023 | Fistula | 2 | Patient |
| 2023 | Failure of Implant | 385 | Patient |
| 2023 | Bone Fracture(s) | 1 | Patient |
| 2023 | Abscess | 5 | Patient |
| 2023 | Patient Device Interaction Problem | 28 | Device |
| 2023 | Osseointegration Problem | 11 | Device |
| 2023 | Migration | 5 | Device |
| 2023 | Mechanical Problem | 4 | Device |
| 2023 | Loss of Osseointegration | 52 | Device |
| 2023 | Insufficient Information | 8 | Device |
| 2023 | Fracture | 1 | Device |
| 2023 | Failure to Osseointegrate | 267 | Device |
| 2023 | Difficult to Insert | 5 | Device |
| 2023 | Device Markings/Labelling Problem | 3 | Device |
| 2023 | Adverse Event Without Identified Device or Use Problem | 16 | Device |
| 2023 | Activation, Positioning or Separation Problem | 3 | Device |
| 2022 | Unspecified Infection | 12 | Patient |
| 2022 | Pain | 16 | Patient |
| 2022 | Numbness | 2 | Patient |
| 2022 | Failure of Implant | 103 | Patient |
| 2022 | Separation Failure | 2 | Device |
| 2022 | Osseointegration Problem | 26 | Device |
| 2022 | Malposition of Device | 2 | Device |
| 2022 | Loss of Osseointegration | 31 | Device |
| 2022 | Fracture | 12 | Device |
| 2022 | Failure to Osseointegrate | 271 | Device |
| 2022 | Failure to Deliver | 1 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 21 | Device |
| 2022 | Activation, Positioning or Separation Problem | 2 | Device |
| 2021 | Insufficient Information | 2 | Device |
| 2021 | Failure to Osseointegrate | 20 | Device |
| 2020 | Failure of Implant | 2 | Patient |
| 2020 | Failure to Osseointegrate | 2 | Device |
| 2020 | Device Markings/Labelling Problem | 1 | Device |