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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: NOBEL BIOCARE AB BRÅNEMARK SYSTEM MK III TIU NP 3.3X15MM; ENDOSSEOUS DENTAL IMPLANT

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NOBEL BIOCARE AB BRÅNEMARK SYSTEM MK III TIU NP 3.3X15MM; ENDOSSEOUS DENTAL IMPLANT Back to Search Results
Model Number 28909
Medical Device Problem Code Loss of Osseointegration (2408)
Health Effect - Clinical Code Failure of Implant (1924)
Date of Event 05/26/2023
Type of Reportable Event Serious Injury
Event or Problem Description
Implant failed due to a loss of osseointegration.
 
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Brand Name
BRÅNEMARK SYSTEM MK III TIU NP 3.3X15MM
Common Device Name
ENDOSSEOUS DENTAL IMPLANT
Manufacturer (Section D)
NOBEL BIOCARE AB
dimbovägen 2
karlskoga 69151
SW  69151
MDR Report Key17185658
Report Number2027971-2023-091801
Device Sequence Number6332881
Product Code DZE
UDI-Device Identifier07332747001143
UDI-Public(01)07332747001143(10)12028356(17)190904
Combination Product (Y/N)N
Initial Reporter CountrySW
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2011
Device Explanted Year2023
Serviced by Third Party (Y/N)N
Reporter Type Importer
Initial Reporter Occupation Dentist
Type of Report Initial
Report Date (Section F) 06/22/2023
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 Date09/04/2019
Device Model Number28909
Device Catalogue Number28909
Device Lot Number12028356
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Was the Report Sent to FDA? No
Distributor Facility Aware Date06/21/2023
Event Location Outpatient Treatment Facility
Initial Date Received by Manufacturer Not provided
Initial Report FDA Received Date06/22/2023
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 Age71 YR
Patient SexMale
Date Report Sent to FDA06/22/2023
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