CLEAR-LOCK RETAINERS FOR LIFE NI

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2018-08-09 for CLEAR-LOCK RETAINERS FOR LIFE NI manufactured by Prismatik Dentalcraft, Inc..

Event Text Entries

[116703235] Date of event was not specified; however, the patient used reported device some time in between (b)(6) 2018 to (b)(6) 2018. The device was received and the evaluation is anticipated. Once the investigation is completed, a supplemental report will be submitted. This report is for the 5th of 6 reported devices for the same patient: please reference 3011649314-2018-00264 ((b)(4)) for the 1st device. Please reference 3011649314-2018-00265 ((b)(4)) for the 2nd device. Please reference 3011649314-2018-00266 ((b)(4)) for the 3rd device. Please reference 3011649314-2018-00267 ((b)(4)) for the 4th device. Please reference 3011649314-2018-00269 ((b)(4)) for the 6th device.
Patient Sequence No: 1, Text Type: N, H10


[116703236] This report is for the 3rd upper retainer: it was reported that the patient experienced adverse reaction while using the clear lock retainer appliances. The patient reported of erythema on the area near tooth # 12 and # 13 and the right lateral area of the tongue. The patient also reported of burning sensation at tip of the tongue. The patient tried over the counter alcohol free mouth wash and hydrogen peroxide with no change in symptoms. The patient requested antiviral medication as symptoms were similar to her previous viral outbreak in the past. Valtrex was prescribed but it made her sick. Xylocaine was also prescribed, which only helped for an hour at a time. The patient experienced irritation with retainers since she began to use the devices in (b)(6) 2018 to (b)(6) 2018. The patient stopped using the devices in (b)(6) 2018 when there was no change to the patient's symptoms. The dentist made adjustment to the upper retainers to move away from the tissue on the palate on the upper left. Patient was recommended to clean the retainers using warm water and soft toothbrush. The patient has no known allergies; however, the patient has had dry mouth at night occasionally for years. The patient reported to be taking several medications: sertraline 25mg for years, crestor 5mg, baby aspirin 82mg and nutrafol supplements (4 tabs per day).
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3011649314-2018-00268
MDR Report Key7770824
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2018-08-09
Date of Report2018-11-08
Date Mfgr Received2018-11-08
Device Manufacturer Date2018-03-10
Date Added to Maude2018-08-09
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationDENTIST
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. TOAN HOANG
Manufacturer Street2212 DUPONT DRIVE SUITE P
Manufacturer CityIRVINE CA 92612
Manufacturer CountryUS
Manufacturer Postal92612
Manufacturer Phone9492251235
Manufacturer G1PRISMATIK DENTALCRAFT, INC.
Manufacturer Street2212 DUPONT DRIVE SUITE P
Manufacturer CityIRVINE CA 92612
Manufacturer CountryUS
Manufacturer Postal Code92612
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCLEAR-LOCK RETAINERS FOR LIFE
Generic NameRETAINER
Product CodeDYJ
Date Received2018-08-09
Returned To Mfg2018-07-11
Model NumberNI
Catalog NumberNI
Lot NumberNI
OperatorLAY USER/PATIENT
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerPRISMATIK DENTALCRAFT, INC.
Manufacturer Address2212 DUPONT DRIVE SUITE P IRVINE CA 92612 US 92612


Patients

Patient NumberTreatmentOutcomeDate
101. Other; 2. Required No Informationntervention 2018-08-09

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