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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: NOBEL BIOCARE AB NOBELSPEEDY SHORTY NP Ø3.3MM; ENDOSSEOUS DENTAL IMPLANT

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NOBEL BIOCARE AB NOBELSPEEDY SHORTY NP Ø3.3MM; ENDOSSEOUS DENTAL IMPLANT Back to Search Results
Model Number 37609
Medical Device Problem Code Failure to Osseointegrate (1863)
Health Effect - Clinical Codes Failure of Implant (1924); Pain (1994)
Date of Event 09/15/2022
Type of Reportable Event Serious Injury
Event or Problem Description
Implant failed due to a failure to osseointegrate.
 
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Brand Name
NOBELSPEEDY SHORTY NP Ø3.3MM
Common Device Name
ENDOSSEOUS DENTAL IMPLANT
Manufacturer (Section D)
NOBEL BIOCARE AB
dimbovägen 2
karlskoga 69151
SW  69151
MDR Report Key15775677
Report Number2027971-2022-131361
Device Sequence Number6601129
Product Code DZE
UDI-Device Identifier07332747086287
UDI-Public(01)07332747086287(10)12086456(17)220416
Combination Product (Y/N)N
Initial Reporter CountryJA
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2022
Device Explanted Year2022
Serviced by Third Party (Y/N)N
Reporter Type Importer
Initial Reporter Occupation Dentist
Type of Report Initial
Report Date (Section F) 11/10/2022
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 Date04/16/2022
Device Model Number37609
Device Catalogue Number37609
Device Lot Number12086456
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Was the Report Sent to FDA? No
Distributor Facility Aware Date11/07/2022
Event Location Outpatient Treatment Facility
Initial Date Received by Manufacturer Not provided
Initial Report FDA Received Date11/10/2022
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 Age58 YR
Patient SexFemale
Date Report Sent to FDA11/10/2022
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