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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience
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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
BIOMET FRANCE S.A.R.L. GTS STANDARD FEMORAL STEM SIZE +1 01/15/2019
ENCORE MEDICAL L.P. X-ALT HIP 01/07/2019
ZIMMER BIOMET, INC. CONTINUUM TM SHELL WITH CLUSTER HOLES PO 08/13/2018
ENCORE MEDICAL L.P. X-ALT HIP 07/24/2018
ZIMMER BIOMET, INC. NEUTRAL LINER 32 MM I.D. SIZE HH FOR USE 05/02/2018
STELKAST INC. EXP ACETABULAR SHELL AND LINER 03/05/2018
STELKAST INC. PROVIDENT HIP SYSTEM 03/01/2018
ENCORE MEDICAL L.P X-ALT HIP 07/06/2017
ENCORE MEDICAL, L.P. X-ALT HIP 03/10/2017
ENCORE MEDICAL, L.P. X-ALT HIP 12/05/2016
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