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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: BIOHORIZONS INC. BIOHORIZONS INC.; DENTAL IMPLANT

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BIOHORIZONS INC. BIOHORIZONS INC.; DENTAL IMPLANT Back to Search Results
Model Number TTLY3010
Medical Device Problem Code Failure to Osseointegrate (1863)
Health Effect - Clinical Code Insufficient Information (4580)
Date of Event 05/20/2026
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 Key25561328
Report Number1060818-2026-12401
Device Sequence Number18640671
Product Code DZE
UDI-Device Identifier00847236009540
UDI-Public00847236009540
Combination Product (Y/N)N
Initial Reporter CountryIT
PMA/510(K) Number
K223697
Number of Events Summarized1
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
Report Date (Section B) 06/19/2026
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 Expiration Date04/13/2026
Device Model NumberTTLY3010
Device Catalogue NumberTTLY3010
Device Lot Number2102396
Is the Reporter a Health Professional? Yes
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 05/20/2026
Initial Report FDA Received Date06/19/2026
Date Device Manufactured04/14/2021
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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