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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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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, MP8, HXE-PLUS, 36M 03/01/2024
ENCORE MEDICAL L.P LINER 10 DEG. HOODED NEU, MP8 HXE-PLUS, 02/29/2024
ZIMMER BIOMET, INC. 32MM I.D. SIZE KK NEUTRAL LINER USE WITH 02/13/2024
ZIMMER BIOMET, INC. 32MM I.D. SIZE KK NEUTRAL LINER 02/12/2024
ENCORE MEDICAL L.P LINER 10 DEG HOODED-NEU, MP11, HXE-PLUS, 12/12/2023
ENCORE MEDICAL L.P. LINER/NON-HOODED-NEU, MP6, HXE-PLUS, 32M 12/07/2023
ENCORE MEDICAL L.P. LINER 10 DEG HOODED-NEU, MP9, HXE-PLUS, 11/07/2023
ENCORE MEDICAL L.P LINER 10 DEG. HOODED NEU, MP7, HXE-PLUS, 10/20/2023
ENCORE MEDICAL L.P LINER/NON-HOODED-NEU, MP9, HXE-PLUS, 40M 09/15/2023
ENCORE MEDICAL L.P LINER 10 DEG. HOODED NEU, MP8 HXE-PLUS, 07/20/2023
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