MANDIBULAR ANTERIOR REPOSITIONING APPLIANCE (MARA)

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 2015-03-13 for MANDIBULAR ANTERIOR REPOSITIONING APPLIANCE (MARA) manufactured by Allesee Orthodontic Appliances.

Event Text Entries

[20785273] A doctor's office alleged that a patient had experienced sores in the mouth while wearing a mara appliance.
Patient Sequence No: 1, Text Type: D, B5


[21070428] The dentist prescribed peroxyl and orabase for treatment of the sores. It was confirmed that the patient has fully recovered and is doing fine. A new appliance will be fabricated with consideration to patient comfort.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2184045-2015-00004
MDR Report Key4600657
Report Source05
Date Received2015-03-13
Date of Report2015-02-18
Date Mfgr Received2015-02-18
Date Added to Maude2015-03-13
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 FDA0
Event Location0
Manufacturer ContactMRS. KERRI CASINO
Manufacturer Street1717 W COLLINS AVE
Manufacturer CityORANGE CA 92867
Manufacturer CountryUS
Manufacturer Postal92867
Manufacturer Phone7145167634
Manufacturer G1ALLESEE ORTHODONTIC APPLIANCES
Manufacturer Street13931 SPRING STREET
Manufacturer CitySTURTEVANT WI 53177
Manufacturer CountryUS
Manufacturer Postal Code53177
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMANDIBULAR ANTERIOR REPOSITIONING APPLIANCE (MARA)
Generic NamePOSITIONER, TOOTH, PREFORMED
Product CodeKMY
Date Received2015-03-13
ID NumberWO# 7763092
OperatorOTHER
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerALLESEE ORTHODONTIC APPLIANCES
Manufacturer Address13931 SPRING STREET STURTEVANT WI 53177 US 53177


Patients

Patient NumberTreatmentOutcomeDate
101. Other; 2. Required No Informationntervention 2015-03-13

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.