MAUDE Adverse Event Report: ZIMMER DENTAL IMPL TAPERED SP 4.8MM 10M M OCTAGON; DENTAL IMPLANT

Catalog Number	SPWB10
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Unspecified Infection (1930)
Type of Reportable Event	Serious Injury
Event or Problem Description
It was reported that the implants were placed on tooth locations 45 and 46, 3 months later they achived osteonintegration.Loaded 4 or 5 months later without any issues.In 2021 infection was noticed and it was treated with antiobitics.Curettage was performed in 2022.In 2023 the issue became worst and the implants were lost due to peri-implantitis in 2024.Inflammation and abscess reported as a consequence of the event.This report refers to 2022 infection.
Additional Manufacturer Narrative
Zimvie complaint number: (b)(4).A4: patient weight: unknown / not provided.B3: date of event: unknown / not provided.D10: concomitant medical product: spb10, impl tapered sp 3.7mm 10m m octagon, (b)(6).D10: therapy date: unknown / not provided.G4: premarket identification: k011245|k002188.A summary investigation has been completed for infection events identifying that a definitive root cause cannot be identified due to the wide range of external (non-design/ non-manufacturing related) factors potentially impacting the sterility of the implant and its environment.Should additional information be received which indicates that the device may have caused or contributed to the infection event, an additional report will be submitted.
Additional Manufacturer Narrative
Zimvie complaint number (b)(4).Additional report to update the placement date to unknown.The following fields have been updated: b4: date of this report.B5: describe event or problem.D6a.If implanted, give date : updated to unknown.G3: date received by manufacturer.G6: type of report.H1: type of reportable event.H2: follow up type.H3: device evaluated by manufacturer.H6: adverse event problem.H10: additional narrative.A summary investigation has been completed for infection events identifying that a definitive root cause cannot be identified due to the wide range of external (non-design/ non-manufacturing related) factors potentially impacting the sterility of the implant and its environment.Should additional information be received which indicates that the device may have caused or contributed to the infection event, an additional report will be submitted.H3 other text: summary investigation.
Event or Problem Description
No further event information is available at the time of this report.

• Brand Name: IMPL TAPERED SP 4.8MM 10M M OCTAGON
• Common Device Name: DENTAL IMPLANT
• Manufacturer (Section D): ZIMMER DENTAL; 4555 riverside drive; palm beach gardens FL 33410
• Manufacturer (Section G): ZIMMER DENTAL; 4555 riverside drive; palm beach gardens FL 33410
• Manufacturer Contact: carlos gordian-arroyo ; 4555 riverside drive; palm beach gardens, FL 33410 ; 5619713230
• MDR Report Key: 21207974
• Report Number: 0002023141-2025-00185
• Device Sequence Number: 8071312
• Product Code: DZE
• UDI-Device Identifier: 00889024017566
• UDI-Public: (01)00889024017566(17)240723(10)2019071246
• Combination Product (Y/N): N
• Initial Reporter Country: FR
• PMA/510(K) Number: K082639
• Exemption Number: 5645646
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2018
• Device Explanted Year: 2024
• 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): 05/01/2025

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: Lay User/Patient
• Device Expiration Date: 07/23/2024
• Device Catalogue Number: SPWB10
• Device Lot Number: 2019071246
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: Not provided
• Supplement Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 01/22/2025
• Supplement Report FDA Received Date: 05/02/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 07/23/2019
• 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
• Concomitant Medical Products and Therapy/Usage Dates: DENTAL IMPLANT SEE H10 NARRATIVE.
• Patient Age: 55 YR
• Patient Sex: Male
• Patient Ethnicity: Non Hispanic