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 | 14 | Patient |
| 2024 | Pain | 13 | Patient |
| 2024 | Osteomyelitis | 2 | Patient |
| 2024 | Numbness | 4 | Patient |
| 2024 | Insufficient Information | 2 | Patient |
| 2024 | Inflammation | 2 | Patient |
| 2024 | Implant Pain | 1 | Patient |
| 2024 | Foreign Body In Patient | 4 | Patient |
| 2024 | Fistula | 6 | Patient |
| 2024 | Failure of Implant | 587 | Patient |
| 2024 | Bone Fracture(s) | 8 | Patient |
| 2024 | Abscess | 21 | Patient |
| 2024 | Premature Separation | 4 | Device |
| 2024 | Osseointegration Problem | 16 | Device |
| 2024 | Naturally Worn | 2 | Device |
| 2024 | Migration | 3 | Device |
| 2024 | Material Deformation | 2 | Device |
| 2024 | Malposition of Device | 2 | Device |
| 2024 | Loss of Osseointegration | 47 | Device |
| 2024 | Fracture | 7 | Device |
| 2024 | Failure to Osseointegrate | 350 | Device |
| 2024 | Difficult to Remove | 1 | Device |
| 2024 | Difficult to Insert | 2 | Device |
| 2024 | Device Markings/Labelling Problem | 2 | Device |
| 2024 | Adverse Event Without Identified Device or Use Problem | 32 | Device |
| 2024 | Activation, Positioning or Separation Problem | 2 | Device |
| 2023 | Unspecified Infection | 24 | Patient |
| 2023 | Paresthesia | 2 | Patient |
| 2023 | Pain | 61 | Patient |
| 2023 | Osteomyelitis | 2 | Patient |
| 2023 | Numbness | 14 | Patient |
| 2023 | Insufficient Information | 4 | Patient |
| 2023 | Inflammation | 2 | Patient |
| 2023 | Hypersensitivity/Allergic reaction | 1 | Patient |
| 2023 | Foreign Body In Patient | 5 | Patient |
| 2023 | Fistula | 2 | Patient |
| 2023 | Failure of Implant | 461 | Patient |
| 2023 | Bone Fracture(s) | 2 | Patient |
| 2023 | Abscess | 4 | Patient |
| 2023 | Premature Separation | 1 | Device |
| 2023 | Patient Device Interaction Problem | 47 | Device |
| 2023 | Osseointegration Problem | 14 | Device |
| 2023 | Migration | 5 | Device |
| 2023 | Mechanical Problem | 2 | Device |
| 2023 | Malposition of Device | 4 | Device |
| 2023 | Loss of Osseointegration | 72 | Device |
| 2023 | Insufficient Information | 4 | Device |
| 2023 | Fracture | 3 | Device |
| 2023 | Failure to Osseointegrate | 314 | Device |
| 2023 | Difficult to Remove | 2 | Device |
| 2023 | Difficult to Insert | 4 | Device |
| 2023 | Device Markings/Labelling Problem | 3 | Device |
| 2023 | Adverse Event Without Identified Device or Use Problem | 18 | Device |
| 2023 | Activation, Positioning or Separation Problem | 6 | Device |
| 2022 | Unspecified Infection | 14 | Patient |
| 2022 | Pain | 19 | Patient |
| 2022 | Failure of Implant | 102 | Patient |
| 2022 | Abscess | 2 | Patient |
| 2022 | Separation Failure | 2 | Device |
| 2022 | Osseointegration Problem | 41 | Device |
| 2022 | Material Deformation | 2 | Device |
| 2022 | Loss of Osseointegration | 22 | Device |
| 2022 | Insufficient Information | 4 | Device |
| 2022 | Fracture | 2 | Device |
| 2022 | Failure to Osseointegrate | 320 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 31 | Device |
| 2021 | Unspecified Infection | 2 | Patient |
| 2021 | Pain | 2 | Patient |
| 2021 | Failure of Implant | 16 | Patient |
| 2021 | Fracture | 4 | Device |
| 2021 | Failure to Osseointegrate | 18 | Device |
| 2021 | Adverse Event Without Identified Device or Use Problem | 2 | Device |
| 2020 | Failure of Implant | 2 | Patient |
| 2020 | Failure to Osseointegrate | 2 | Device |