LUCITONE FRS RESIN 904855

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2016-07-09 for LUCITONE FRS RESIN 904855 manufactured by Dentsply Prosthetics.

Event Text Entries

[49124333] While it is unknown if the device used in this case caused or contributed to the patient's symptoms, it is possible as allergic reactions to dental materials are known and reported, with medical consequences being dependent upon the severity of the individual allergic response and subsequent exposure to the same material. Therefore, this event meets the criteria for reportability per 21 cfr part 803. The device was not returned for evaluation and the lot number was not provided for retained-product testing and/or dhr review.
Patient Sequence No: 1, Text Type: N, H10


[49124334] It was reported that a patient was developing ulcers after one to two days of wearing dentures that were fashioned with lucitone frs. The patient is under the care of a gp who is currently investigating the possible cause.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2585114-2016-00002
MDR Report Key5781034
Report SourceFOREIGN,HEALTH PROFESSIONAL
Date Received2016-07-09
Date of Report2016-06-08
Date Mfgr Received2016-06-08
Date Added to Maude2016-07-09
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 ContactMRS. HELEN LEWIS
Manufacturer Street221 W. PHILADELPHIA ST. SUITE 60W
Manufacturer CityYORK PA 17401
Manufacturer CountryUS
Manufacturer Postal17401
Manufacturer Phone7178494229
Manufacturer G1DENTSPLY PROSTHETICS
Manufacturer Street570 WEST COLLEGE AVENUE
Manufacturer CityYORK PA 17404
Manufacturer CountryUS
Manufacturer Postal Code17404
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameLUCITONE FRS RESIN
Generic NameRESIN, DENTURE, RELINING, REPAIRING, REBASING
Product CodeEBI
Date Received2016-07-09
Model NumberNA
Catalog Number904855
Lot NumberUNK
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerDENTSPLY PROSTHETICS
Manufacturer Address570 WEST COLLEGE AVENUE YORK PA 17404 US 17404


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2016-07-09

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