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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: UNKNOWN TMJ; JOINT, TEMPOROMANDIBULAR, IMPLANT

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UNKNOWN TMJ; JOINT, TEMPOROMANDIBULAR, IMPLANT Back to Search Results
Device Problem Use of Device Problem (1670)
Patient Problems Headache (1880); High Blood Pressure/ Hypertension (1908); Discomfort (2330); Difficulty Chewing (4522)
Event Date 03/04/2008
Event Type  Injury  
Event Description
A reporter called to report adverse events she has been experiencing ever since she had tmj implant for her lower parts of teeth.She said from the day she had the implant, she has been having headaches, her blood pressure goes up.She said even talking hurts so bad and she can't chew good.She said it feels so tight.She said the doctor who did the implant who was really good, treated her for 3 years and left the practice.She said she is not having proper treatment from her replacement doctor.She said she had an mri, but it did not show anything problematic.
 
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Brand Name
TMJ
Type of Device
JOINT, TEMPOROMANDIBULAR, IMPLANT
Manufacturer (Section D)
UNKNOWN
MDR Report Key17315678
MDR Text Key319045765
Report NumberMW5119312
Device Sequence Number1
Product Code LZD
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 07/12/2023
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
Is the Reporter a Health Professional? No
Initial Date Manufacturer Received Not provided
Initial Date FDA Received07/12/2023
Patient Sequence Number1
Patient Age79 YR
Patient SexFemale
Patient Weight64 KG
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