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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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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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111 records meeting your search criteria returned- Product Code: HSX Patient Problem: No Information Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
MATERIALISE USA LLC. ZIMMER PATIENT SPECIFIC INSTRUMENT 05/05/2015
ZIMMER INC. ZIMMER UNICOMPARTMENTAL FEMORAL COMPONEN 03/27/2015
ZIMMER, INC. ZUK ARTICULAR SURFACE 10/22/2014
ZIMMER, INC. NEXGEN TIBIAL AUGMENT BLOCK 09/24/2014
DEPUY ORTHOPAEDICS, INC. UNKNOWN DEPUY FEMORAL COMPONENT 09/19/2014
SMITH & NEPHEW, INC. GENESISII TIBIAL INSERT AND FEMORAL COMP 09/15/2014
BLUE BELT TECHNOLOGIES STRIDE 06/11/2014
BLUE BELT TECHNOLOGIES STRIDE 06/11/2014
CONFORMIS IUNI G2 05/28/2014
CONFORMIS IUNI G2 02/19/2014
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