DAMON COPPER NITI WIRE

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a other report with the FDA on 2015-10-28 for DAMON COPPER NITI WIRE manufactured by Ormco Corporation.

Event Text Entries

[29727086] It was alleged that a patient swallowed a wire and surgical intervention may have been required; however no further specific information has been received at this time. An update will be provided upon receipt of new information.
Patient Sequence No: 1, Text Type: N, H10


[29727087] It was alleged that a patient swallowed damon cuniti wire.
Patient Sequence No: 1, Text Type: D, B5


[36554781] .
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2016150-2015-00021
MDR Report Key5184184
Report SourceOTHER
Date Received2015-10-28
Date of Report2015-10-08
Date Mfgr Received2015-10-08
Date Added to Maude2015-10-28
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA0
Report to FDA3
Event Location3
Manufacturer ContactMRS. SUZETTE RAMPAIR-JOHNSON
Manufacturer Street1332 SOUTH LONE HILL AVE.
Manufacturer CityGLENDORA CA 91740
Manufacturer CountryUS
Manufacturer Postal91740
Manufacturer Phone9099625730
Manufacturer G1ORMCO CORPORATION
Manufacturer Street1332 SOUTH LONE HILL AVENUE
Manufacturer CityGLENDORA CA 91740
Manufacturer CountryUS
Manufacturer Postal Code91740
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameDAMON COPPER NITI WIRE
Generic NameWIRE, ORTHODONTIC
Product CodeDZC
Date Received2015-10-28
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerORMCO CORPORATION
Manufacturer Address1332 SOUTH LONE HILL AVENUE GLENDORA CA 91740 US 91740


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2015-10-28

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