FDA Adverse Event
Injury
Summary report: N
2027971-2022-043110
MDR report key: 13563074
·
Received February 18, 2022
Report
- Report Number
- 2027971-2022-043110
- Event Type
- Injury
- Date Received
- February 18, 2022
- Date of Event
- January 27, 2022
- Manufacturer
- NOBEL BIOCARE USA, LLC
- Product Code
- DZE
- PMA / PMN Number
- K073142
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- US
- Reporter Occupation
- DENTIST
- Health Professional
- Yes
Narratives
Description of Event or Problem · 0
IMPLANT FAILED DUE TO A FAILURE TO OSSEOINTEGRATE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 529313 | DZE | NOBEL BIOCARE USA, LLC |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 72 YR | Male | Required Intervention |