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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: TMJ SOLUTIONS, LLC DBA TMJ CONCEPTS TMJ BILATERAL IMPLANTS; PATIENT-FITTED TMJ RECONSTRUCTION PROSTHESIS

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TMJ SOLUTIONS, LLC DBA TMJ CONCEPTS TMJ BILATERAL IMPLANTS; PATIENT-FITTED TMJ RECONSTRUCTION PROSTHESIS Back to Search Results
Catalog Number CHG020
Device Problem Device Dislodged or Dislocated (2923)
Patient Problem Joint Dislocation (2374)
Event Date 01/29/2024
Event Type  Injury  
Event Description
It was reported that the left side tmj device was dislocated and a second surgery will be performed to reduce the dislocation.
 
Manufacturer Narrative
Device is not available for evaluation.If additional information is received it will be reported on a supplemental report.H3 other text : implanted.
 
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Brand Name
TMJ BILATERAL IMPLANTS
Type of Device
PATIENT-FITTED TMJ RECONSTRUCTION PROSTHESIS
Manufacturer (Section D)
TMJ SOLUTIONS, LLC DBA TMJ CONCEPTS
6059 king drive
ventura 93003
Manufacturer (Section G)
TMJ SOLUTIONS, LLC DBA TMJ CONCEPTS
6059 king drive
ventura 93003
Manufacturer Contact
rylee koole
6059 king drive
ventura 93003
8056503391
MDR Report Key18692205
MDR Text Key335187627
Report Number0002031049-2024-00012
Device Sequence Number1
Product Code LZD
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
P980052
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Company Representative
Reporter Occupation Other
Type of Report Initial
Report Date 02/12/2024
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received02/12/2024
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Catalogue NumberCHG020
Device Lot Number2302021048
Was Device Available for Evaluation? No
Date Manufacturer Received01/29/2024
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Patient Sequence Number1
Patient Outcome(s) Required Intervention;
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