FDA Adverse Event Injury Summary report: N

BIOHORIZONS INC.

MDR report key: 23351432 · Received October 21, 2025

Report

Report Number
1060818-2025-34442
Event Type
Injury
Date Received
October 21, 2025
Date of Event
September 23, 2025
Report Date
November 19, 2025
Manufacturer
BIOHORIZONS INC.
Product Code
DZE
UDI-DI
00847236024178
PMA / PMN Number
K071638
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IL, 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
225969 BIOHORIZONS INC. DENTAL IMPLANT DZE BIOHORIZONS INC. CTA4609 2404064 00847236024178

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Required Intervention