FDA Adverse Event Injury Summary report: N

ET NH DENTAL IMPLANT

MDR report key: 19911909 · Received August 5, 2024

Report

Report Number
3007135442-2024-00009
Event Type
Injury
Date Received
August 5, 2024
Report Date
March 13, 2024
Manufacturer
HIOSSEN, INC.
Product Code
DZE
PMA / PMN Number
K151526
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
DENTIST
Health Professional
Yes

Narratives

Description of Event or Problem · 0

DENTAL IMPLANT FAILURE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2274271 ET NH DENTAL IMPLANT DENTAL IMPLANT DZE HIOSSEN, INC. ET3R4010B H1E22H292

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Required Intervention