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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
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7 records meeting your search criteria returned- Product Code: GXQ Product Problem: Device Appears to Trigger Rejection Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
COOK BIOTECH BIODESIGN DURAL GRAFT 07/01/2021
MEDTRONIC NEUROSURGERY DUREPAIR DURA SUBSTITUTE 06/03/2020
AESCULAP AG LYOPLANT ONLAY 2.5X2.5CM 03/11/2020
AESCULAP AG LYOPLANT ONLAY 2.5X2.5CM 03/05/2020
AESCULAP AG LYOPLANT ONLAY 5.0X5.0CM 03/03/2020
NATUS NEURO INCORPORATED DURAFORM 06/27/2019
NATUS NEURO INCORPORATED DURAFORM 06/27/2019
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