TRANSCEND 2000 CERAMIC BRACKET 2001-XXX

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2002-06-25 for TRANSCEND 2000 CERAMIC BRACKET 2001-XXX manufactured by 3m Unitek.

Event Text Entries

[246831] Orthodontist reported that during the debonding of a transcend 2000 ceramic bracket, the buccal cusp of tooth #1-5 (upper right second bicuspid) fractured. The tooth will be repaired with a crown.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2020467-2002-00008
MDR Report Key401808
Report Source05
Date Received2002-06-25
Date of Report2002-06-12
Date of Event2002-05-10
Date Mfgr Received2002-06-12
Date Added to Maude2002-06-28
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location0
Manufacturer ContactMARLYN SCHEFF
Manufacturer Street2724 SOUTH PECK ROAD
Manufacturer CityMONROVIA CA 91016
Manufacturer CountryUS
Manufacturer Postal91016
Manufacturer Phone6265744496
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTRANSCEND 2000 CERAMIC BRACKET
Generic NameORTHODONTIC CERAMIC BRACKET
Product CodeDYW
Date Received2002-06-25
Model NumberNA
Catalog Number2001-XXX
Lot NumberUNK
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key390842
Manufacturer3M UNITEK
Manufacturer Address2724 SOUTH PECK RD. MONROVIA CA 91016 US
Baseline Brand NameTRANSCEND 2000 CERAMIC BRACKET
Baseline Generic NameORTHODONTIC CERAMIC BRACKET
Baseline Model NoNA
Baseline Catalog No2001-XXX
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2002-06-25

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