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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
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7 records meeting your search criteria returned- Product Code: LXT Product Problem: Device Slipped Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
SYNTHES GMBH 2.8 THRD GUIDE WIRE- TROCAR POINT 300 07/27/2023
BIOMET ORTHOPEDICS LP NON LOCK 2.7MM X 22MM 03/17/2015
BIOMET ORTHOPEDICS DVR EPAK NARROW LOCK PLATE R 02/20/2015
BIOMET ORTHOPEDICS DVR EPAK LOCK PLT L 10/31/2014
BIOMET ORTHOPEDICS MD SCREW 2.7MM X 24MM STE 10/31/2014
BIOMET ORTHOPEDICS PEG SCREW 10/30/2014
BIOMET ORTHOPEDICS UNKNOWN LOCK SCREW 06/05/2014
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