FDA Adverse Event
Injury
Summary report: N
2027971-2026-083922
MDR report key: 25307184
·
Received May 27, 2026
Report
- Report Number
- 2027971-2026-083922
- Event Type
- Injury
- Date Received
- May 27, 2026
- Date of Event
- March 21, 2026
- Report Date
- May 27, 2026
- Manufacturer
- NOBEL BIOCARE USA, LLC
- Product Code
- DZE
- Adverse Event
- Yes
- Report Source
- Distributor report
- Reporter Location
- CH
- Reporter Occupation
- DENTIST
- Health Professional
- Yes
Narratives
Description of Event or Problem · 0
FAILURE TO OSSEOINTEGRATE
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 248205 | DZE | NOBEL BIOCARE USA, LLC |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |