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MAUDE Adverse Event Report: BIOHORIZONS INC. BIOHORIZONS INC.; DENTAL IMPLANT
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BIOHORIZONS INC. BIOHORIZONS INC.; DENTAL IMPLANT
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Model Number
TLXP4610
Medical Device Problem Code
Failure to Osseointegrate (1863)
Health Effect - Clinical Code
Insufficient Information (4580)
Date of Event
02/09/2026
Type of Reportable Event
Serious Injury
Event or Problem Description
Implant failed to osseointegrate.
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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
24519460
Report Number
1060818-2026-04190
Device Sequence Number
9746316
Product Code
DZE
UDI-Device Identifier
00847236021993
UDI-Public
00847236021993
Combination Product (Y/N)
N
Initial Reporter Country
UK
Number of Events Summarized
1
Summary Report (Y/N)
N
Device Implanted Year
2025
Device Explanted Year
2025
Serviced by Third Party (Y/N)
N
Reporter Type
Manufacturer
Report Source
Company Representative
Initial Reporter Occupation
Dentist
Type of Report
Initial
Report Date
(Section B)
03/11/2026
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
TLXP4610
Device Catalogue Number
TLXP4610
Device Lot Number
2500514
Is the Reporter a Health Professional?
Yes
Type of Report(Section G)
Thirty-Day
Initial Date Received by Manufacturer
02/09/2026
Initial Report FDA Received Date
03/05/2026
Date Device Manufactured
01/23/2025
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
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