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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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5 records meeting your search criteria returned- Product Code: IQI Patient Problem: No Patient Involvement Report Date From: 01/1/2015
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ManufacturerBrand NameDate Report Received
DJO, LLC PROCARE MOBILIMB L4 09/05/2019
BREG, INC. JWALKER BOOT 07/13/2017
BREG, INC. JWALKER BOOT 06/22/2017
BREG, INC. JWALKER BOOT 04/19/2017
BREG, INC. JWALKER BOOT 03/10/2017
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