FDA Adverse Event Injury Summary report: N

ANK IMPL A11 D3,5 MM/L11 MM

MDR report key: 19729815 · Received July 12, 2024

Report

Report Number
3013111692-2024-20726
Event Type
Injury
Date Received
July 12, 2024
Date of Event
September 9, 2022
Report Date
August 6, 2024
Manufacturer
DENTSPLY IMPLANTS MANUFACTURING GMBH
Product Code
DZE
PMA / PMN Number
K140347
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
GM
Reporter Occupation
DENTIST
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

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.

Additional Manufacturer Narrative · 0

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 IMPL A11 D3,5 MM/L11 MM CATALOG # 31010210. THIS IS A FOLLOW UP REPORT FOR THIS CORRECTED INFORMATION. CORRECTING UDI # FROM (B)(4) TO UNK. THIS IS A FOLLOW UP REPORT FOR THIS CORRECTED INFORMATION.

Description of Event or Problem · 0

IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2444331 ANK IMPL A11 D3,5 MM/L11 MM IMPLANT, ENDOSSEOUS, ROOT-FORM DZE DENTSPLY IMPLANTS MANUFACTURING GMBH UNK

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Required Intervention