THERMOFORM RETAINER 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 2019-02-25 for THERMOFORM RETAINER NI manufactured by Prismatik Dentalcraft, Inc..

Event Text Entries

[137114632] Patient's weight was asked but unknown. Multiple follow-ups were conducted to obtain additional information on the event; however, requested information has not been provided. Reported device was returned for evaluation. Once the evaluation is completed and new information is obtained, a supplemental report will be submitted.
Patient Sequence No: 1, Text Type: N, H10


[137114633] It was reported that a patient experienced an allergic reaction to the thermoform retainer after the first use. The patient reported of bumps breaking out around her tongue. The patient has known nickel allergy.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3011649314-2019-00016
MDR Report Key8368658
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2019-02-25
Date of Report2019-05-29
Date Mfgr Received2019-05-29
Device Manufacturer Date2019-01-23
Date Added to Maude2019-02-25
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 NameTHERMOFORM RETAINER
Generic NameTHERMOFORM RETAINER
Product CodeDYJ
Date Received2019-02-25
Returned To Mfg2019-02-06
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 2019-02-25

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