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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: INSTITUT STRAUMANN AG S, Ø 3.3MM RN, SLACT. 10MM, TIZR, GEF.; ENDOSSEOUS DENTAL IMPLANT
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INSTITUT STRAUMANN AG S, Ø 3.3MM RN, SLACT. 10MM, TIZR, GEF.; ENDOSSEOUS DENTAL IMPLANT Back to Search Results
Catalog Number 033.432G
Medical Device Problem Code Failure to Osseointegrate (1863)
Health Effect - Clinical Codes Pain (1994); Tissue Damage (2104)
Date of Event 06/28/2019
Type of Reportable Event Serious Injury
Event or Problem Description
The clinician reports the implant was inserted (b)(6) 2019 in fdi 37 of the patient's mouth.Details of surgery: bone overheating.On (b)(6) 2019, non-osseointegration was verified.Patient presented with inadequate bone quality/quantity.The device was forwarded to the manufacturer.At the event the patient experienced: pain and mobility.No further patient complications were reported.
 
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Brand Name
S, Ø 3.3MM RN, SLACT. 10MM, TIZR, GEF.
Common Device Name
ENDOSSEOUS DENTAL IMPLANT
Manufacturer (Section D)
INSTITUT STRAUMANN AG
peter merian-weg 12
basel 04002
CH  04002
MDR Report Key9036451
Report Number0009613348-2019-09325
Device Sequence Number2528083
Product Code DZE
UDI-Device Identifier07630031715579
UDI-Public07630031715579
Combination Product (Y/N)N
PMA/510(K) Number
K090260
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2019
Device Explanted Year2019
Reporter Type Manufacturer
Report Source foreign,health professional
Initial Reporter Occupation Dentist
Type of Report Initial
Report Date (Section B) 09/13/2019
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 Date09/06/2022
Device Catalogue Number033.432G
Device Lot NumberNP820
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer07/24/2019
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer Not provided
Initial Report FDA Received Date09/13/2019
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 Age41 YR
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