ANK C/X IMPL A11/D3.5/L11
Report
- Report Number
- 3013111692-2024-23547
- Event Type
- Injury
- Date Received
- August 5, 2024
- Date of Event
- January 11, 2024
- Report Date
- August 30, 2024
- Manufacturer
- DENTSPLY IMPLANTS MANUFACTURING GMBH
- Product Code
- DZE
- PMA / PMN Number
- K140347
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- LG
- Reporter Occupation
- DENTIST
- Health Professional
- Yes
Narratives
ADDITIONAL FDA CODING BEING ADDED AFTER INVESTIGATION OF DEVICE. ADDING ADDITIONAL TYPE OF INVESTIGATION CODE 10. THIS IS A FOLLOW UP REPORT TO ADD THIS ADDITIONAL CODE. DEVICE RECEIVED FOR THIS EVENT IS BEING CORRECTED FROM ANK C/X IMPL A9.5/D3.5/L9.5 CATALOG # 17-0543 TO ANK C/X IMPL A11/D3.5/L11 CATALOG # 31010410. THIS IS A FOLLOW UP REPORT FOR THIS CORRECTED INFORMATION. CORRECTING UDI # FROM (B)(4). THIS IS A FOLLOW UP REPORT FOR THIS CORRECTED INFORMATION.
THEREFORE, BECAUSE A SERIOUS INJURY RESULTED, THIS EVENT IS REPORTABLE PER 21 CFR PART 803. SECTION H6 WAS DONE BASED ON THE INFORMATION PROVIDED BY THE INITIAL REPORTER AND OUR LONG-TIME EXPERIENCE IN THE INVESTIGATION OF SIMILAR COMPLAINTS. PRODUCT RETURN IS REQUESTED AND PRODUCT WILL BE EVALUATED AFTER RECEIPT. IN CASE ANY NEW OR ADDITIONAL INFORMATION WILL BE GAINED FROM THIS INVESTIGATION A FOLLOW-UP REPORT WILL BE SENT. TREND IS TRACKED AND MONITORED.
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1844766 | ANK C/X IMPL A11/D3.5/L11 | IMPLANT, ENDOSSEOUS, ROOT-FORM | DZE | DENTSPLY IMPLANTS MANUFACTURING GMBH | B140008567 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown | Required Intervention |