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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: NOBEL BIOCARE AB NOBELPARALLEL CC TIULTRA RP 4.3X11.5MM; ENDOSSEOUS DENTAL IMPLANT

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NOBEL BIOCARE AB NOBELPARALLEL CC TIULTRA RP 4.3X11.5MM; ENDOSSEOUS DENTAL IMPLANT Back to Search Results
Model Number 300305
Device Problem Defective Device (2588)
Patient Problem Failure of Implant (1924)
Event Date 03/23/2023
Event Type  Injury  
Event Description
The implant malfunctioned due to an engagement issue.The malfunction did not cause or contribute to a death or serious injury.
 
Event Description
The initial report did not have the correct event type documented, the correct event type, injury, is provided in this follow up report.
 
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Brand Name
NOBELPARALLEL CC TIULTRA RP 4.3X11.5MM
Type of Device
ENDOSSEOUS DENTAL IMPLANT
Manufacturer (Section D)
NOBEL BIOCARE AB
dimbovägen 2
karlskoga 69151
SW  69151
MDR Report Key16716522
MDR Text Key313061764
Report Number2027971-2023-062314
Device Sequence Number1
Product Code DZE
UDI-Device Identifier07332747127973
UDI-Public(01)07332747127973(10)12204691(17)270716
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Distributor
Reporter Occupation Dentist
Type of Report Initial,Followup
Report Date 04/11/2023
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? Yes
Device Operator Health Professional
Device Model Number300305
Device Catalogue Number300305
Device Lot Number12204691
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Was the Report Sent to FDA? No
Date Report Sent to FDA04/11/2023
Distributor Facility Aware Date03/27/2023
Event Location Outpatient Treatment Facility
Initial Date Manufacturer Received Not provided
Initial Date FDA Received04/11/2023
Supplement Dates Manufacturer ReceivedNot provided
Supplement Dates FDA Received09/07/2023
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage A
Patient Sequence Number1
Patient Outcome(s) Required Intervention;
Patient Age79 YR
Patient SexMale
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