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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: BIOMET 3I OSSEOTITE¿ TAPERED CERTAIN¿ IMPLANT 5 X 10MM; DENTAL IMPLANT

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BIOMET 3I OSSEOTITE¿ TAPERED CERTAIN¿ IMPLANT 5 X 10MM; DENTAL IMPLANT Back to Search Results
Catalog Number XIFNT510
Medical Device Problem Code Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes Unspecified Infection (1930); Pain (1994); Osteolysis (2377)
Date of Event 03/12/2025
Type of Reportable Event Serious Injury
Additional Manufacturer Narrative
Zimvie complaint number (b)(4).A4: patient weight: unknown / not provided.A summary investigation has been completed for peri-implantitis events recognizing that a definitive root cause cannot be identified due to a wide range of external factors (non-design or manufacturing related), including medical conditions (e.G., diabetes, poor bone quality, etc.) / patient habits (e.G., smoking) and surgical technique.Previously completed investigations for these events have not identified any signals indicating potential non-conformances affecting the manufacturing and sterilization processes.Furthermore, the probability of a manufacturing or design defect that might lead to peri-implantitis occurring and escaping the available detections has been assessed and found remote and almost nonexistent.Should additional information be received which indicates that the device may have caused or contributed to the event, an additional report will be submitted.
 
Event or Problem Description
The doctor reports that the dental implant located in dental position number # 26 failed due to peri-implantitis.The doctor reports in the per that the procedure was not concluded by placing another implant.Pain was reported as a result of the event.
 
Additional Manufacturer Narrative
Zimvie complaint number (b)(4).The following fields have been updated: b5: describe event or problem.E: initial reported corrected.G6: type of report.H2: follow up type.H10: additional narrative.
 
Event or Problem Description
No further event information is available at the time of this report.
 
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Brand Name
OSSEOTITE¿ TAPERED CERTAIN¿ IMPLANT 5 X 10MM
Common Device Name
DENTAL IMPLANT
Manufacturer (Section D)
BIOMET 3I
4555 riverside drive
palm beach gardens FL 33410
Manufacturer (Section G)
BIOMET 3I
4555 riverside drive
palm beach gardens FL 33410
Manufacturer Contact
carlos gordian-arroyo
4555 riverside drive
palm beach gardens, FL 33410
5619713230
MDR Report Key22025705
Report Number0001038806-2025-01074
Device Sequence Number20617050
Product Code DZE
UDI-Device Identifier00844868022008
UDI-Public(01)00844868022008(17)260928(10)2021090642
Combination Product (Y/N)N
Initial Reporter CountrySP
PMA/510(K) Number
K130949
Exemption Number5645646
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2022
Device Explanted Year2025
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source Foreign,Health Professional
Initial Reporter Occupation Dentist
Type of Report Initial,Followup
Report Date (Section B) 05/15/2025
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 Other
Device Expiration Date09/28/2026
Device Catalogue NumberXIFNT510
Device Lot Number2021090642
Was Device Available for Evaluation? No
Date Returned to Manufacturer04/23/2025
Is the Reporter a Health Professional? Yes
Type of Report(Section G)Initial
Initial Date Received by Manufacturer Not provided
Supplement Date Received by ManufacturerNot provided
Initial Report FDA Received Date05/15/2025
Supplement Report FDA Received Date05/15/2025
Was Device Evaluated by Manufacturer? (Y/N) Yes
Date Device Manufactured09/28/2021
Is the Device Labeled for Single Use? (Y/N) No
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Usage of Device Unknown
Patient Sequence Number1
Outcome Attributed to Adverse Event Required Intervention;
Patient Age60 YR
Patient SexUnknown
Patient EthnicityNon Hispanic
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