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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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4 records meeting your search criteria returned- Product Code: GXQ Product Problem: Lack of Effect Report Date From: 01/1/2019

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ManufacturerBrand NameDate Report Received
INTEGRA - PRINCETON DURAGEN DURAL GRAFT MATRIX 01/26/2024
INTEGRA - PRINCETON DURAGEN 4X5 1 PACK CE 01/12/2024
INTEGRA - PRINCETON DURAGEN 3X3 1 PACK CE 06/23/2023
INTEGRA - PRINCETON DURAGEN-UNKNOWN PRODUCT ID 06/15/2023
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