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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: NOBEL BIOCARE AB GÖTEBORG BRÅNEMARK SYSTEM® ZYGOMA TIUNITE 50MM; ENDOSSEOUS DENTAL IMPLANT

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NOBEL BIOCARE AB GÖTEBORG BRÅNEMARK SYSTEM® ZYGOMA TIUNITE 50MM; ENDOSSEOUS DENTAL IMPLANT Back to Search Results
Catalog Number 34739
Medical Device Problem Code Failure to Osseointegrate (1863)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 12/22/2025
Type of Reportable Event Serious Injury
Event or Problem Description
Failure to osseointegrate.
 
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Brand Name
BRÅNEMARK SYSTEM® ZYGOMA TIUNITE 50MM
Common Device Name
ENDOSSEOUS DENTAL IMPLANT
Manufacturer (Section D)
NOBEL BIOCARE AB GÖTEBORG
västra hamngatan 1
göteborg 41117
SW  41117
MDR Report Key24782397
Report Number2027971-2026-064210
Device Sequence Number10037045
Product Code DZE
UDI-Device Identifier07332747160215
UDI-Public(01)07332747160215(10)12161313(17)250906
Combination Product (Y/N)N
Initial Reporter CountryCH
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2025
Device Explanted Year2026
Serviced by Third Party (Y/N)N
Reporter Type Importer
Initial Reporter Occupation Dentist
Type of Report Initial
Report Date (Section F) 04/03/2026
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 Date09/06/2025
Device Catalogue Number34739
Device Lot Number12161313
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Was the Report Sent to FDA? No
Distributor Facility Aware Date03/26/2026
Event Location Outpatient Treatment Facility
Initial Date Received by Manufacturer Not provided
Initial Report FDA Received Date04/03/2026
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Usage of Device A
Patient Sequence Number1
Outcome Attributed to Adverse Event Required Intervention;
Patient Age69 YR
Patient SexMale
Date Report Sent to FDA04/03/2026
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