FDA Adverse Event Injury Summary report: N

IMP,TSV,MCOL MG,3.7MM,10M

MDR report key: 25120847 · Received May 8, 2026

Report

Report Number
0001038806-2026-02528
Event Type
Injury
Date Received
May 8, 2026
Date of Event
February 3, 2025
Report Date
May 8, 2026
Manufacturer
ZIMVIE US CORP LLC
Product Code
DZE
UDI-DI
00889024019720
PMA / PMN Number
K111889
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
SP
Reporter Occupation
DENTIST
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

ZIMVIE COMPLAINT NUMBER (B)(4). A1: PATIENT IDENTIFIER: UNKNOWN / NOT PROVIDED. A4: PATIENT WEIGHT: UNKNOWN / NOT PROVIDED. D10: CONCOMITANT MEDICAL PRODUCT: TSVMB10, IMP,TSV,MCOL MG,3.7MM,10M, LOT: 1241673. 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.

Description of Event or Problem · 0

IT WAS REPORTED THE IMPLANTS AT TOOTH SITE #37-42 WERE REMOVED DUE TO PERIIMPLANTITIS. PROCEDURE WAS COMPLETED WITH OTHER IMPLANTS. BONE TYPE: ILL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
31961 IMP,TSV,MCOL MG,3.7MM,10M DENTAL IMPLANT DZE ZIMVIE US CORP LLC 1241673 00889024019720

Patients

Seq Age Sex Outcome Treatment
1