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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 LINER/NON-HOODED-NEU, MP6, HXE-PLUS, 32M 06/26/2023
ENCORE MEDICAL L.P LINER/NON-HOODED-NEU, MP7, HXE-PLUS, 36M 05/05/2023
ENCORE MEDICAL L.P LINER 10 DEG HOODED-NEU, MP9, HXE-PLUS, 03/31/2023
ENCORE MEDICAL L.P. LINER 10 DEG HOODED-NEU, MP9, HXE-PLUS, 03/23/2023
ENCORE MEDICAL L.P X-ALT HIP 12/30/2022
ENCORE MEDICAL L.P X-ALT HIP 11/30/2022
ENCORE MEDICAL L.P. X-ALT HIP 11/15/2022
ENCORE MEDICAL L.P. X-ALT HIP 11/15/2022
ENCORE MEDICAL L.P. X-ALT HIP 11/15/2022
ENCORE MEDICAL L.P. X-ALT HIP 09/15/2022
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