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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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13 records meeting your search criteria returned- Product Code: LXH Patient Problem: Foreign Body Reaction Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
ARTHREX, INC. unknown brand name 01/10/2024
SMITH & NEPHEW, INC. BONE ANCHORS WITH ARTHROSCOPIC DELIVERY 11/01/2023
DEPUY ORTHOPAEDICS INC US REPLICA A STEM 12.0MM 03/13/2023
ARTHREX, INC. FIBERTAK DISPOSABLES STRAIGHT KIT 03/06/2023
DEPUY MITEK LLC US EXPRESSEW III NEEDLE PK5 06/11/2018
MEDOS INTERNATIONAL SàRL CH 1.45MM NITINOL GUIDEWIRE BLUNT 04/17/2018
DEPUY MITEK LLC US EXPRESSEW III NEEDLE PK5 04/09/2018
DEPUY MITEK EXPRESSEW III NEEDLE PK5 02/08/2018
DEPUY MITEK LLC US ACL DISPOSABLES KIT 12/15/2017
DEPUY MITEK LLC US ACL DISPOSABLES KIT 12/15/2017
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