MAUDE Adverse Event Report: ZIMVIE US CORP LLC T3 NON-PLATFORM SWITCHED TAPERED IMPLANT 3.25 X 13MM; DENTAL IMPLANT

Catalog Number	BOST3213
Medical Device Problem Code	Fracture (1260)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	10/13/2025
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Zimvie complaint number (b)(4).A2: age at time of the event unknown / not provided.A4: patient weight unknown / not provided.D6: d6a.If implanted, unknown.
Event or Problem Description
It was reported the implant, at tooth site #22, fractured at the body.Implant was removed completely.Procedure was completed.
Additional Manufacturer Narrative
Zimvie complaint number (b)(4).Zimvie received one (1) bost3213, (t3® non-platform switched tapered implant 3.25 x 13mm) for evaluation.Visual evaluation was performed; the implant shows extensive signs of wear/use.Damage is likely caused during removal.Bone debris can be observed on its external threads.Unknown fracture screw fragment identified stuck inside of it.Additional information was obtained on 15-jan-2026 regarding the inspection findings.The customer confirmed that the screw fractured during the removal process.The unknown screw was recorded as a concomitant.Dhr review was completed for the subject lot number 2016091029.No deviations or non-conformances, which could have caused or contributed to the reported event, were noted as part of the dhr.Complaint history review was performed for the reported lot number 2016091029 for similar events and no other complaint was identified.Review completed utilizing keywords: ¿dental : functional : fracture : implant¿ based on the investigation and risk management file review, the most likely root cause determined from the investigation was patient factors.Therefore, based on the available information, a device malfunction did occur.The implant was fractured at the collar.The reported event was confirmed.No further investigation or immediate capa / hhe/d escalation is required, as the complaint investigation did not confirm the products were nonconforming at the time of distribution, and no new failure mode, harm, or hazardous situation was identified through the investigation performed.At this time, the complaint investigation has been completed and the record will be closed.If additional information is received, the record will be re-opened for further evaluation.
Event or Problem Description
No further event information is available at the time of this report.

• Brand Name: T3 NON-PLATFORM SWITCHED TAPERED IMPLANT 3.25 X 13MM
• Common Device Name: DENTAL IMPLANT
• Manufacturer (Section D): ZIMVIE US CORP LLC; 4555 riverside drive; palm beach gardens FL 33410
• Manufacturer (Section G): ZIMVIE US CORP LLC; 4555 riverside drive; palm beach gardens FL 33410
• Manufacturer Contact: mark mashburn ; 4555 riverside drive; palm beach gardens, FL 33410 ; 5619713230
• MDR Report Key: 23654367
• Report Number: 0001038806-2025-03411
• Device Sequence Number: 10054958
• Product Code: DZE
• UDI-Device Identifier: 00844868028895
• UDI-Public: (01)00844868028895(17)210926(10)2016091029
• Combination Product (Y/N): N
• Initial Reporter Country: SP
• PMA/510(K) Number: K122300
• Exemption Number: 5645646
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Explanted Year: 2025
• 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): 02/19/2026

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?: Yes
• Operator of Device: Other
• Device Expiration Date: 09/26/2021
• Device Catalogue Number: BOST3213
• Device Lot Number: 2016091029
• Was Device Available for Evaluation?: No
• Date Returned to Manufacturer: 11/05/2025
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Follow-Up
• Initial Date Received by Manufacturer: Not provided
• Supplement Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 11/26/2025
• Supplement Report FDA Received Date: 02/19/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 09/26/2016
• 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 Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Sex: Unknown
• Patient Ethnicity: Non Hispanic