FDA Adverse Event Injury Summary report: N

BIOHORIZONS INC.

MDR report key: 23209419 · Received October 3, 2025

Report

Report Number
1060818-2025-33369
Event Type
Injury
Date Received
October 3, 2025
Date of Event
September 4, 2025
Report Date
October 27, 2025
Manufacturer
BIOHORIZONS INC.
Product Code
DZE
UDI-DI
00847236012397
PMA / PMN Number
K223697
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IT
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
319322 BIOHORIZONS INC. DENTAL IMPLANT DZE BIOHORIZONS INC. BTA4210 2306011 00847236012397

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Required Intervention