NOBELACTIVE INTERNAL RP 5.0X10MM

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 22 Patient
2024 Sinus Perforation 4 Patient
2024 Pain 44 Patient
2024 Osteomyelitis 2 Patient
2024 Numbness 4 Patient
2024 Implant Pain 3 Patient
2024 Foreign Body In Patient 1 Patient
2024 Failure of Implant 420 Patient
2024 Bone Fracture(s) 4 Patient
2024 Abscess 8 Patient
2024 Premature Separation 4 Device
2024 Osseointegration Problem 4 Device
2024 Migration 1 Device
2024 Malposition of Device 4 Device
2024 Loss of Osseointegration 146 Device
2024 Fracture 4 Device
2024 Failure to Osseointegrate 157 Device
2024 Device Markings/Labelling Problem 9 Device
2024 Adverse Event Without Identified Device or Use Problem 10 Device
2024 Activation, Positioning or Separation Problem 1 Device
2023 Unspecified Infection 45 Patient
2023 Pain 77 Patient
2023 Osteopenia/ Osteoporosis 1 Patient
2023 Numbness 24 Patient
2023 Insufficient Information 1 Patient
2023 Implant Pain 1 Patient
2023 Foreign Body In Patient 3 Patient
2023 Fistula 3 Patient
2023 Failure of Implant 665 Patient
2023 Bone Fracture(s) 3 Patient
2023 Separation Failure 4 Device
2023 Patient Device Interaction Problem 18 Device
2023 Osseointegration Problem 23 Device
2023 Migration 3 Device
2023 Mechanical Problem 3 Device
2023 Material Deformation 2 Device
2023 Malposition of Device 1 Device
2023 Loss of Osseointegration 219 Device
2023 Insufficient Information 1 Device
2023 Fracture 16 Device
2023 Failure to Osseointegrate 355 Device
2023 Difficult to Remove 2 Device
2023 Difficult to Insert 1 Device
2023 Adverse Event Without Identified Device or Use Problem 10 Device
2022 Unspecified Infection 23 Patient
2022 Pain 35 Patient
2022 Numbness 7 Patient
2022 Foreign Body In Patient 1 Patient
2022 Failure of Implant 210 Patient
2022 Separation Failure 1 Device
2022 Patient Device Interaction Problem 2 Device
2022 Osseointegration Problem 51 Device
2022 Migration 1 Device
2022 Malposition of Device 2 Device
2022 Loss of Osseointegration 218 Device
2022 Insufficient Information 2 Device
2022 Fracture 16 Device
2022 Failure to Osseointegrate 339 Device
2022 Device Damaged by Another Device 2 Device
2022 Adverse Event Without Identified Device or Use Problem 22 Device
2021 Pain 2 Patient
2021 Insufficient Information 2 Patient
2021 Failure of Implant 37 Patient
2021 Osseointegration Problem 8 Device
2021 Malposition of Device 3 Device
2021 Loss of Osseointegration 32 Device
2021 Fracture 6 Device
2021 Failure to Osseointegrate 88 Device
2020 Pain 2 Patient
2020 Failure of Implant 14 Patient
2020 Osseointegration Problem 2 Device
2020 Failure to Osseointegrate 23 Device