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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
BIOMET UK LTD. DELTA CERAMIC FEM HD 36/0MM 02/25/2021
BIOMET UK LTD. DELTA CER FEM HD 32/0MM T1 02/23/2021
ENCORE MEDICAL L.P X-ALT HIP 01/05/2021
ENCORE MEDICAL L.P. X-ALT HIP 12/18/2020
Unknown Manufacturer LINER, ACETABULAR, HOODED, NEUTRAL, 10 D 09/23/2020
ENCORE MEDICAL L.P. X-ALT HIP 09/11/2020
ENCORE MEDICAL L.P. X-ALT HIP 08/21/2020
ENCORE MEDICAL L.P. X-ALT HIP 05/29/2020
ZIMMER BIOMET, INC. TPRLC 133 FP TYPE1 PPS HO 8.0 04/07/2020
ENCORE MEDICAL L.P. FMP HIP 03/26/2020
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