BRÅNEMARK SYSTEM MK III TIU RP 3.75X10MM Adverse Event — Injury (MDR 2027971-2020-11096)
BRÅNEMARK SYSTEM MK III TIU RP 3.75X10MM Adverse Event — Injury (MDR 2027971-2020-11096) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: BRÅNEMARK SYSTEM MK III TIU RP 3.75X10MM; Generic name: ENDOSSEOUS DENTAL IMPLANT; Manufacturer: NOBEL BIOCARE AB.
| Device | BRÅNEMARK SYSTEM MK III TIU RP 3.75X10MM |
|---|---|
| Generic name | ENDOSSEOUS DENTAL IMPLANT |
| Manufacturer | NOBEL BIOCARE AB |
| Report number | 2027971-2020-11096 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-28 |
| Narrative | IMPLANT FAILED DUE TO FAILURE TO OSSEOINTEGRATE. |
| Source | openFDA MAUDE (device adverse events) |
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