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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: IKZ Product Problem: Unintended Movement Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
ARJOHUNTLEIGH, INC. ROTOPRONE 06/27/2019
ARJOHUNTLEIGH, INC. ROTOPRONE 03/15/2019
ARJOHUNTLEIGH, INC. ROTOPRONE 05/11/2017
ARJOHUNTLEIGH ROTOPRONE 06/22/2015
ARJOHUTNLEIGH, INC SPIRIT SELECT 01/12/2015
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