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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: Unspecified Infection Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
DJO LLC LONG THUMB SPICA II (LTSII), FOREARM BAS 06/23/2021
3M HEALTH CARE ACE OPEN PATELLA KNEE SUPPORT 06/01/2020
OSSUR MEXICO UNLOADER ONE X 04/15/2020
BREG, INC. BREG HIP RECOVERY BRACE 12/16/2015
DEROYAL INDUSTRIES TRANSITION POST-OP KNEE BRACE 03/13/2015
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