FDA Adverse Event Injury Summary report: N

BIOHORIZONS INC.

MDR report key: 23646571 · Received November 25, 2025

Report

Report Number
1060818-2025-36796
Event Type
Injury
Date Received
November 25, 2025
Date of Event
October 28, 2025
Report Date
January 24, 2026
Manufacturer
BIOHORIZONS INC.
Product Code
DZE
UDI-DI
00847236012403
PMA / PMN Number
K223697
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
PA, 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
2146816 BIOHORIZONS INC. DENTAL IMPLANT DZE BIOHORIZONS INC. BTA4212 2405311 00847236012403

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Required Intervention