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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: BIOHORIZONS BIOHORIZONS; DENTAL IMPLANT

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BIOHORIZONS BIOHORIZONS; DENTAL IMPLANT Back to Search Results
Model Number TLX3010
Medical Device Problem Code Failure to Osseointegrate (1863)
Health Effect - Clinical Code Insufficient Information (4580)
Date of Event 11/13/2025
Type of Reportable Event Serious Injury
Event or Problem Description
Implant failed to osseointegrate.
 
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Brand Name
BIOHORIZONS
Common Device Name
DENTAL IMPLANT
Manufacturer (Section D)
BIOHORIZONS
2300 riverchase ctr
birmingham AL 35244
Manufacturer Contact
2300 riverchase ctr
birmingham, AL 35244
MDR Report Key23780142
Report Number1060818-2025-37804
Device Sequence Number10076048
Product Code DZE
UDI-Device Identifier00847236022457
UDI-Public00847236022457
Combination Product (Y/N)N
Initial Reporter CountryCA
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2018
Device Explanted Year2025
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) 12/13/2025
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 Expiration Date04/13/2022
Device Model NumberTLX3010
Device Catalogue NumberTLX3010
Device Lot Number1702048
Was Device Available for Evaluation? Yes
Is the Reporter a Health Professional? Yes
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 11/13/2025
Initial Report FDA Received Date12/11/2025
Was Device Evaluated by Manufacturer? (Y/N) Yes
Date Device Manufactured04/14/2017
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 Number1
Outcome Attributed to Adverse Event Required Intervention;
Patient SexUnknown
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