MAUDE Adverse Event Report: BioHorizons, Inc. BioHorizons, Inc.; Dental Implant

Model Number	BTR4212
Medical Device Problem Code	Failure to Osseointegrate (1863)
Health Effect - Clinical Code	Insufficient Information (4580)
Date of Event	05/19/2026
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
This initial emdr record was due for submission originally on 6/18/2026.The delay resulted from an internal processing oversight within our workflow.Upon identification of the delayed submission, immediate submission is taking place, along with a review to determine if any additional records due 6/18/2026 have been addressed.The review confirmed no additional impact reports were found.
Event or Problem Description
Implant failed to osseointegrate.

• Brand Name: BioHorizons, Inc.
• Common Device Name: Dental Implant
• Manufacturer (Section D): BioHorizons, Inc.; 2300 riverchase center; birmingham AL 35244
• Manufacturer (Section G): BioHorizons Inc.; 2300 riverchase center; birmingham AL 35244
• Manufacturer Contact: anissa smith ; 2300 riverchase center; birmingham, AL 35244
• MDR Report Key: 25699476
• Report Number: 1060818-2026-13545
• Device Sequence Number: 21269195
• Product Code: DZE
• UDI-Device Identifier: 00847236021856
• UDI-Public: 00847236021856
• Combination Product (Y/N): N
• Initial Reporter Country: SP
• PMA/510(K) Number: K223697
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Initial Reporter Occupation: Dentist
• Type of Report: Initial,Followup
• Report Date (Section B): 10/01/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Model Number: BTR4212
• Device Catalogue Number: BTR4212
• Device Lot Number: 2506909
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 05/19/2026
• Supplement Date Received by Manufacturer: 06/29/2026
• Initial Report FDA Received Date: 07/02/2026
• Supplement Report FDA Received Date: 10/01/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 12/15/2025
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Sex: Unknown