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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ALLESEE ORTHODONTIC APPLIANCES HERBST; BITE-JUMPING ORTHODONTIC APPLIANCE

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ALLESEE ORTHODONTIC APPLIANCES HERBST; BITE-JUMPING ORTHODONTIC APPLIANCE Back to Search Results
Device Problem Insufficient Information (3190)
Patient Problem Inflammation (1932)
Event Type  Injury  
Event Description
A doctor alleged that a patient had experienced gum inflammation while wearing a herbst appliance.
 
Manufacturer Narrative
The doctor removed the appliance, gave the patient samples of peroxyl, and recommended salt water rinses for treatment.To date, the patient has fully recovered and is doing fine.A new appliance will be fabricated with consideration to patient comfort.
 
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Brand Name
HERBST
Type of Device
BITE-JUMPING ORTHODONTIC APPLIANCE
Manufacturer (Section D)
ALLESEE ORTHODONTIC APPLIANCES
13931 spring street
sturtevant WI 53177
Manufacturer (Section G)
ALLESEE ORTHODONTIC APPLIANCES
13931 spring street
sturtevant WI 53177
Manufacturer Contact
kerri casino
1717 west collins avenue
orange, CA 92867
7145167634
MDR Report Key3944909
MDR Text Key15812140
Report Number2184045-2014-00004
Device Sequence Number1
Product Code EJF
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
K923405
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Health Professional
Reporter Occupation Other
Type of Report Initial
Report Date 06/25/2014
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received07/18/2014
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Other
Other Device ID NumberWO #7583354
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Date Manufacturer Received06/25/2014
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Date Device Manufactured10/17/2013
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Patient Sequence Number1
Patient Outcome(s) Other; Required Intervention;
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