FDA Adverse Event Injury Summary report: N

BIOHORIZONS INC.

MDR report key: 23347097 · Received October 21, 2025

Report

Report Number
1060818-2025-34360
Event Type
Injury
Date Received
October 21, 2025
Date of Event
September 23, 2025
Report Date
November 17, 2025
Manufacturer
BIOHORIZONS INC.
Product Code
DZE
UDI-DI
00847236013707
PMA / PMN Number
K223697
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
NC, US
Reporter Occupation
DENTIST
Health Professional
Yes

Narratives

Description of Event or Problem · 0

IMPLANT FAILED TO OSSEOINTEGRATE.

Description of Event or Problem · 0

IMPLANT FAILED TO OSSEOINTEGRATE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1000150 BIOHORIZONS INC. DENTAL IMPLANT DZE BIOHORIZONS INC. BTA3809 2302744 00847236013707

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Required Intervention