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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
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81 records meeting your search criteria returned- Product Code: JWH Product Problem: Device Damaged Prior to Use Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
STELKAST INC. EXP TIBIAL INSERTS AND PATELLAR COMPONEN 11/16/2017
AESCULAP IMPLANT SYSTEMS AS COLUMBUS CR/PS TIB.PLAT.CEMENTED T3 11/14/2017
STELKAST INC. EXP TIBIAL INSERTS AND PATELLAR COMPONEN 11/06/2017
ZIMMER ORTHOPAEDIC MFG. LTD. NEXGEN LPS-FLEX OPTION GSF FEMORAL COMPO 08/23/2016
ZIMMER INC NEXGEN STEMMED TIBIAL COMPONENT 02/18/2016
ZIMMER INC NEXGEN LPS-FLEX ARTICULAR SURFACE 01/05/2016
STRYKER ORTHOPAEDICS-MAHWAH GMRS PROXIMAL TIBIAL STANDARD 01/27/2015
ZIMMER NEXGEN MIS STEMMED TIBIAL COMPONENT 04/03/2014
ZIMMER MANUFACTURING B.V. NEXGEN STEMMED TIBIAL COMPONENT PRECOAT 03/05/2014
ZIMMER, INC. NEXGEN CR ARTICULAR SURFACE 02/26/2014
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