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 | 93 | Patient |
| 2024 | Swelling/ Edema | 60 | Patient |
| 2024 | Sinus Perforation | 1 | Patient |
| 2024 | Pain | 162 | Patient |
| 2024 | Numbness | 1 | Patient |
| 2024 | Inflammation | 50 | Patient |
| 2024 | Increased Sensitivity | 2 | Patient |
| 2024 | Hypersensitivity/Allergic reaction | 5 | Patient |
| 2024 | Hemorrhage/Blood Loss/Bleeding | 28 | Patient |
| 2024 | Fistula | 13 | Patient |
| 2024 | Fibrosis | 263 | Patient |
| 2024 | Abscess | 14 | Patient |
| 2024 | Loss of Osseointegration | 76 | Device |
| 2024 | Fracture | 2 | Device |
| 2024 | Failure to Osseointegrate | 745 | Device |
| 2024 | Adverse Event Without Identified Device or Use Problem | 14 | Device |
| 2023 | Unspecified Infection | 230 | Patient |
| 2023 | Swelling/ Edema | 148 | Patient |
| 2023 | Pain | 354 | Patient |
| 2023 | Numbness | 45 | Patient |
| 2023 | Inflammation | 116 | Patient |
| 2023 | Increased Sensitivity | 19 | Patient |
| 2023 | Hypersensitivity/Allergic reaction | 14 | Patient |
| 2023 | Hemorrhage/Blood Loss/Bleeding | 138 | Patient |
| 2023 | Fistula | 31 | Patient |
| 2023 | Fibrosis | 638 | Patient |
| 2023 | Abscess | 29 | Patient |
| 2023 | Separation Failure | 2 | Device |
| 2023 | Loss of Osseointegration | 280 | Device |
| 2023 | Fracture | 16 | Device |
| 2023 | Failure to Osseointegrate | 2103 | Device |
| 2023 | Difficult to Insert | 6 | Device |
| 2023 | Adverse Event Without Identified Device or Use Problem | 26 | Device |
| 2022 | Unspecified Infection | 141 | Patient |
| 2022 | Swelling/ Edema | 88 | Patient |
| 2022 | Pain | 220 | Patient |
| 2022 | Numbness | 10 | Patient |
| 2022 | Inflammation | 82 | Patient |
| 2022 | Increased Sensitivity | 12 | Patient |
| 2022 | Hypersensitivity/Allergic reaction | 5 | Patient |
| 2022 | Hemorrhage/Blood Loss/Bleeding | 59 | Patient |
| 2022 | Fistula | 21 | Patient |
| 2022 | Fibrosis | 347 | Patient |
| 2022 | Abscess | 17 | Patient |
| 2022 | Separation Failure | 2 | Device |
| 2022 | Loss of Osseointegration | 538 | Device |
| 2022 | Fracture | 24 | Device |
| 2022 | Failure to Osseointegrate | 3828 | Device |
| 2022 | Difficult to Insert | 13 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 81 | Device |
| 2021 | Unspecified Infection | 2 | Patient |
| 2021 | Swelling/ Edema | 1 | Patient |
| 2021 | Pain | 8 | Patient |
| 2021 | Inflammation | 1 | Patient |
| 2021 | Hemorrhage/Blood Loss/Bleeding | 5 | Patient |
| 2021 | Fibrosis | 3 | Patient |
| 2021 | Loss of Osseointegration | 70 | Device |
| 2021 | Fracture | 3 | Device |
| 2021 | Failure to Osseointegrate | 677 | Device |
| 2021 | Adverse Event Without Identified Device or Use Problem | 4 | Device |
| 2020 | Unspecified Infection | 2 | Patient |
| 2020 | Pain | 1 | Patient |
| 2020 | Failure to Osseointegrate | 23 | Device |