CLARITY METAL-REINFORCED CERAMIC BRACKET 6400-710 OR 6400-711

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 2001-06-04 for CLARITY METAL-REINFORCED CERAMIC BRACKET 6400-710 OR 6400-711 manufactured by 3m Unitek.

Event Text Entries

[228085] Orthodontist reported that during the debonding of a clarity ceramic bracket, tooth dentin was exposed when a piece of enamel approximately 2mm in diameter and 1 to 1/2mm in depth was removed from the buccal surface of an upper right first bicuspid tooth. Orthodontist repaired the tooth with composite material.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2020467-2001-00003
MDR Report Key336015
Report Source05
Date Received2001-06-04
Date of Report2001-05-08
Date of Event2001-05-03
Date Mfgr Received2001-05-08
Date Added to Maude2001-06-07
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 NameCLARITY METAL-REINFORCED CERAMIC BRACKET
Generic NameORTHODONTIC CERAMIC BRACKET
Product CodeDYW
Date Received2001-06-04
Model NumberNA
Catalog Number6400-710 OR 6400-711
Lot NumberUNK
ID Number*
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key325340
Manufacturer3M UNITEK
Manufacturer Address2724 SOUTH PECK ROAD MONROVIA CA 91016 US
Baseline Brand NameCLARITY METAL-REINFORCED CERAMIC BRACKET
Baseline Generic NameORTHODONTIC CERAMIC BRACKET
Baseline Model NoNA
Baseline Catalog No6400-710 OR 6400-711
Baseline ID*


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2001-06-04

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