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U.S. Department of Health and Human Services

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

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HAGER & MEISINGER INFINITY OCTAGON IMPLANT; DENTAL IMPLANT Back to Search Results
Model Number 504108
Medical Device Problem Codes Failure to Osseointegrate (1863); Loss of Osseointegration (2408); Osseointegration Problem (3003); Patient Device Interaction Problem (4001)
Health Effect - Clinical Code Failure of Implant (1924)
Date of Event 03/01/2023
Type of Reportable Event Serious Injury
Event or Problem Description
No integration.
 
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Brand Name
INFINITY OCTAGON IMPLANT
Common Device Name
DENTAL IMPLANT
Manufacturer (Section D)
HAGER & MEISINGER
hansemannstr. 10
neuss, 41468
GM  41468
MDR Report Key17010221
Report Number1287163-2023-54086
Device Sequence Number20591040
Product Code DZE
UDI-Device IdentifierE0HM5041081
UDI-PublicE0HM5041081
Combination Product (Y/N)N
Initial Reporter CountrySP
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2022
Device Explanted Year2023
Serviced by Third Party (Y/N)N
Reporter Type Importer
Initial Reporter Occupation Dentist
Type of Report Initial
Report Date (Section B) 05/26/2023
Report Date (Section F) 05/26/2023
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 Model Number504108
Device Catalogue Number504108
Device Lot NumberB75210
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Was the Report Sent to FDA? Yes
Distributor Facility Aware Date04/28/2023
Device Age1 YR
Event Location Outpatient Treatment Facility
Initial Date Received by Manufacturer Not provided
Initial Report FDA Received Date05/26/2023
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 Age51 YR
Patient SexFemale
Date Report Sent to FDA05/26/2023
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