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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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99 records meeting your search criteria returned- Product Code: OQG Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
STRYKER ORTHOPAEDICS-MAHWAH ACE LINR-E-POLY NEUT-36/54 IMPLANT 07/17/2015
ENCORE MEDICAL, L.P. FMP HIP 05/01/2015
MAKO SURGICAL RSTORIS PST/TFS TOTAL HIP SYSTEM 10/15/2014
MAKO SURGICAL CORP. RESTORIS PST/TFS TOTAL HIP SYSTEM 09/30/2014
MAKO SURGICAL RESTORIS PST/TFS TOTAL HIP SYSTEM 09/19/2014
MAKO SURGICAL RESTORIS PST/TFS TOTAL HIP SYSTEM 07/25/2014
MAKO SURGICAL CORP. RESTORIS PST/TFS TOTAL HIP SYS 05/30/2014
MAKO SURGICAL CORP. RESTORIS PST TOTAL HIP SYSTEM 04/03/2014
MAKO SURGICAL RESTORIS PST TOTAL HIP SYSTEM 03/06/2014
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