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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: HAGER & MEISINGER GMBH INFINITY OCTAGON IMPLANT; DENTAL IMPLANT

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HAGER & MEISINGER GMBH INFINITY OCTAGON IMPLANT; DENTAL IMPLANT Back to Search Results
Model Number 504108
Medical Device Problem Code Patient Device Interaction Problem (4001)
Health Effect - Clinical Code Failure of Implant (1924)
Date of Event 09/29/2021
Type of Reportable Event Serious Injury
Event or Problem Description
Failed to osseointegrate.
 
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Brand Name
INFINITY OCTAGON IMPLANT
Common Device Name
DENTAL IMPLANT
Manufacturer (Section D)
HAGER & MEISINGER GMBH
hansemannstr. 10
41468 neuss, postfach 41429
GM  41429
MDR Report Key16598593
Report Number1287163-2022-53086
Device Sequence Number14780145
Product Code DZE
UDI-Device IdentifierE0HM5041081
UDI-PublicE0HM5041081
Combination Product (Y/N)N
Initial Reporter StateMA
Initial Reporter CountryUS
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2021
Device Explanted Year2021
Serviced by Third Party (Y/N)N
Reporter Type Importer
Initial Reporter Occupation Dentist
Type of Report Initial
Report Date (Section B) 03/23/2023
Report Date (Section F) 11/11/2022
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 Model Number504108
Device Catalogue Number504108
Device Lot NumberB75210
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer11/11/2022
Is the Reporter a Health Professional? Yes
Was the Report Sent to FDA? Yes
Distributor Facility Aware Date11/07/2022
Device Age1 YR
Event Location Outpatient Treatment Facility
Date Report to Manufacturer11/11/2022
Initial Date Received by Manufacturer Not provided
Initial Report FDA Received Date03/23/2023
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Patient Sequence Number1
Outcome Attributed to Adverse Event Required Intervention;
Patient Age56 YR
Patient SexMale
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