BRÅNEMARK SYSTEM MK III TIU RP 3.75X13MM Adverse Event — Injury (MDR 2027971-2020-11003)
BRÅNEMARK SYSTEM MK III TIU RP 3.75X13MM Adverse Event — Injury (MDR 2027971-2020-11003) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: BRÅNEMARK SYSTEM MK III TIU RP 3.75X13MM; Generic name: ENDOSSEOUS DENTAL IMPLANT; Manufacturer: NOBEL BIOCARE AB.
| Device | BRÅNEMARK SYSTEM MK III TIU RP 3.75X13MM |
|---|---|
| Generic name | ENDOSSEOUS DENTAL IMPLANT |
| Manufacturer | NOBEL BIOCARE AB |
| Report number | 2027971-2020-11003 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-28 |
| Narrative | IMPLANT FAILED DUE TO A LOSS OF OSSEOINTEGRATION. |
| Source | openFDA MAUDE (device adverse events) |
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