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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: JDR Product Problem: Unintended Movement Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
DEPUY MITEK LLC US MINI QA+ #2/O OCORD V-5 01/26/2022
CROSSROADS EXTREMITY SYSTEMS DYNAFORCE MPJ SYSTEM 08/12/2019
SMITH & NEPHEW, INC. MNITAC,2.0 TI W/NDL,2#2-0 ULTRABRAID 06/17/2019
WRIGHTS LANE SYNTHES USA PRODUCTS LLC SPEED COMPRESSION IMPLANT KIT 09X07X07MM 10/10/2018
WRIGHTS LANE : SYNTHES USA PRODUCTS LLC STAPLE, FIXATION, BONE 12/14/2017
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