ENDOSSEOUS DENTAL IMPLANT
This device is manufactured by INSTITUT STRAUMANN AG.
The following problems were reported about this device:
| Year | Description | Events/year | Type |
|---|---|---|---|
| 2024 | Unspecified Infection | 38 | Patient |
| 2024 | Swelling/ Edema | 9 | Patient |
| 2024 | Pain | 38 | Patient |
| 2024 | Inflammation | 20 | Patient |
| 2024 | Increased Sensitivity | 2 | Patient |
| 2024 | Hemorrhage/Blood Loss/Bleeding | 11 | Patient |
| 2024 | Fistula | 1 | Patient |
| 2024 | Fibrosis | 82 | Patient |
| 2024 | Abscess | 2 | Patient |
| 2024 | Loss of Osseointegration | 103 | Device |
| 2024 | Fracture | 4 | Device |
| 2024 | Failure to Osseointegrate | 54 | Device |
| 2023 | Unspecified Infection | 235 | Patient |
| 2023 | Swelling/ Edema | 65 | Patient |
| 2023 | Sinus Perforation | 3 | Patient |
| 2023 | Pain | 276 | Patient |
| 2023 | Numbness | 16 | Patient |
| 2023 | Inflammation | 119 | Patient |
| 2023 | Increased Sensitivity | 12 | Patient |
| 2023 | Hypersensitivity/Allergic reaction | 8 | Patient |
| 2023 | Hemorrhage/Blood Loss/Bleeding | 108 | Patient |
| 2023 | Fistula | 22 | Patient |
| 2023 | Fibrosis | 473 | Patient |
| 2023 | Abscess | 28 | Patient |
| 2023 | Loss of Osseointegration | 638 | Device |
| 2023 | Fracture | 45 | Device |
| 2023 | Failure to Osseointegrate | 917 | Device |
| 2023 | Difficult to Insert | 2 | Device |
| 2023 | Adverse Event Without Identified Device or Use Problem | 13 | Device |
| 2022 | Unspecified Infection | 174 | Patient |
| 2022 | Swelling/ Edema | 66 | Patient |
| 2022 | Sinus Perforation | 1 | Patient |
| 2022 | Pain | 204 | Patient |
| 2022 | Numbness | 9 | Patient |
| 2022 | Inflammation | 104 | Patient |
| 2022 | Increased Sensitivity | 12 | Patient |
| 2022 | Hypersensitivity/Allergic reaction | 7 | Patient |
| 2022 | Hemorrhage/Blood Loss/Bleeding | 84 | Patient |
| 2022 | Fistula | 13 | Patient |
| 2022 | Fibrosis | 324 | Patient |
| 2022 | Abscess | 27 | Patient |
| 2022 | Loss of Osseointegration | 1407 | Device |
| 2022 | Fracture | 80 | Device |
| 2022 | Failure to Osseointegrate | 2543 | Device |
| 2022 | Difficult to Insert | 8 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 37 | Device |
| 2021 | Unspecified Infection | 7 | Patient |
| 2021 | Swelling/ Edema | 1 | Patient |
| 2021 | Pain | 5 | Patient |
| 2021 | Numbness | 1 | Patient |
| 2021 | Increased Sensitivity | 1 | Patient |
| 2021 | Hemorrhage/Blood Loss/Bleeding | 4 | Patient |
| 2021 | Fibrosis | 12 | Patient |
| 2021 | Loss of Osseointegration | 152 | Device |
| 2021 | Fracture | 9 | Device |
| 2021 | Failure to Osseointegrate | 357 | Device |
| 2021 | Difficult to Insert | 2 | Device |
| 2021 | Adverse Event Without Identified Device or Use Problem | 2 | Device |
| 2020 | Unspecified Infection | 1 | Patient |
| 2020 | Swelling/ Edema | 1 | Patient |
| 2020 | Pain | 3 | Patient |
| 2020 | Inflammation | 1 | Patient |
| 2020 | Hemorrhage/Blood Loss/Bleeding | 1 | Patient |
| 2020 | Fibrosis | 4 | Patient |
| 2020 | Loss of Osseointegration | 11 | Device |
| 2020 | Failure to Osseointegrate | 13 | Device |