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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
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65 records meeting your search criteria returned- Product Code: IQI Patient Problem: No Known Impact Or Consequence To Patient Report Date From: 01/1/2015
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ManufacturerBrand NameDate Report Received
BREG, INC. ADJUSTAFIT BOOT 06/15/2018
2110420 MUELLER WRIST BRACE 04/05/2018
BREG, INC. JWALKER BOOT 02/16/2018
BREG, INC. JWALKER BOOT 02/02/2018
BREG, INC. ADJUSTAFIT BOOT 01/19/2018
BREG, INC. JWALKER BOOT 01/19/2018
BREG, INC ADJUSTAFIT BOOT 01/08/2018
BREG, INC. JWALKER BOOT 01/08/2018
BREG, INC. JWALKER BOOT 01/08/2018
BREG, INC JWALKER BOOT 11/20/2017
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