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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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3 records meeting your search criteria returned- Product Code: FMP Patient Problem: Injury Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
MIZUHO ORTHOPEDIC SYSTEMS, INC. MIZUHO WILSON FRAME PAD SET 06/24/2020
MEDLINE INDUSTRIES INC HEEL RAISER ULTRA HEEL PROTECTOR 05/09/2017
SPAN AMERICA MEDICAL SYSTEMS, INC. RISK MANAGER 03/13/2015
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