FDA Adverse Event Injury Summary report: N

BIOHORIZONS INC.

MDR report key: 23815294 · Received December 16, 2025

Report

Report Number
1060818-2025-38106
Event Type
Injury
Date Received
December 16, 2025
Date of Event
November 26, 2025
Report Date
April 29, 2026
Manufacturer
BIOHORIZONS INC.
Product Code
DZE
UDI-DI
00847236000592
PMA / PMN Number
K223697
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
SP
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
79705 BIOHORIZONS INC. DENTAL IMPLANT DZE BIOHORIZONS INC. TRX5807 2303544 00847236000592

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Required Intervention