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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
ENCORE MEDICAL L.P. X-ALT HIP 06/10/2021
BIOMET UK LTD. CER OPTION TYPE 1 TPR SLEVE -3 06/08/2021
BIOMET UK LTD. CER BIOLOXD OPTION HD 40MM 06/08/2021
BIOMET UK LTD. DELTA CER FEM HD 28/0MM T1 05/27/2021
BIOMET UK LTD. DELTA CER FEM HD 28/0MM T1 05/27/2021
Unknown Manufacturer LINER 20 DEG HOODED-NEU, MP10, HXE-PLUS, 05/13/2021
Unknown Manufacturer LINER 10 DEG. HOODED NEU, MP8 HXE-PLUS, 05/13/2021
ENCORE MEDICAL L.P X-ALT HIP 04/21/2021
ENCORE MEDICAL L.P. FMP EXTENDED LINERS 03/23/2021
ENCORE MEDICAL L.P. X-ALT HIP 03/11/2021
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