PATIENT-FITTED TMJ RECONSTRUCTION PROSTHESIS TYY-NNNNLM

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-03-19 for PATIENT-FITTED TMJ RECONSTRUCTION PROSTHESIS TYY-NNNNLM manufactured by Tmj Solutions, Inc..

Event Text Entries

[185961941] The surgeon reports patient is doing well.
Patient Sequence No: 1, Text Type: N, H10


[185961942] The surgeon repositioned the left mandibular component due to dislocation.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2031049-2020-00015
MDR Report Key9857463
Report SourceHEALTH PROFESSIONAL
Date Received2020-03-19
Date of Report2020-03-19
Date of Event2020-01-29
Date Mfgr Received2020-02-20
Device Manufacturer Date2019-05-01
Date Added to Maude2020-03-19
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. LORENA LUNDEEN
Manufacturer Street6059 KING DRIVE
Manufacturer CityVENTURA,
Manufacturer CountryUS
Manufacturer Phone6503391
Manufacturer G1TMJ SOLUTIONS, INC.
Manufacturer Street6059 KING DRIVE
Manufacturer CityVENTURA,
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePATIENT-FITTED TMJ RECONSTRUCTION PROSTHESIS
Generic NameLEFT MANDIBULAR COMPONENT
Product CodeLZD
Date Received2020-03-19
Model NumberTYY-NNNNLM
Catalog NumberTYY-NNNNLM
Lot NumberW49184
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerTMJ SOLUTIONS, INC.
Manufacturer Address6059 KING DRIVE VENTURA, US


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-03-19

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.