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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: NOBEL BIOCARE AB GÖTEBORG NOBELREPLACE® STRAIGHT GROOVY WP 5X13MM; ENDOSSEOUS DENTAL IMPLANT

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NOBEL BIOCARE AB GÖTEBORG NOBELREPLACE® STRAIGHT GROOVY WP 5X13MM; ENDOSSEOUS DENTAL IMPLANT Back to Search Results
Catalog Number 32188
Medical Device Problem Code Loss of Osseointegration (2408)
Health Effect - Clinical Codes Failure of Implant (1924); Unspecified Infection (1930)
Date of Event 07/19/2021
Type of Reportable Event Serious Injury
Event or Problem Description
Loss of osseointegration.
 
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Brand Name
NOBELREPLACE® STRAIGHT GROOVY WP 5X13MM
Common Device Name
ENDOSSEOUS DENTAL IMPLANT
Manufacturer (Section D)
NOBEL BIOCARE AB GÖTEBORG
bohusgatan 15
göteborg 41139
SW  41139
MDR Report Key21726197
Report Number2027971-2025-061092
Device Sequence Number17089725
Product Code DZE
UDI-Device Identifier07332747019148
UDI-Public(01)07332747019148(10)662872(17)110115
Combination Product (Y/N)N
Initial Reporter CountryUS
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2006
Device Explanted Year2021
Serviced by Third Party (Y/N)N
Reporter Type Importer
Initial Reporter Occupation Dentist
Type of Report Initial
Report Date (Section F) 03/28/2025
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 Health Professional
Device Expiration Date01/15/2011
Device Catalogue Number32188
Device Lot Number662872
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Was the Report Sent to FDA? No
Distributor Facility Aware Date03/20/2025
Event Location Outpatient Treatment Facility
Initial Date Received by Manufacturer Not provided
Initial Report FDA Received Date03/28/2025
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 Age73 YR
Patient SexFemale
Date Report Sent to FDA03/28/2025
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