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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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11 records meeting your search criteria returned- Product Code: LNQ Patient Problem: Foreign Body Reaction Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
MEDTRONIC NEUROMODULATION ENTERRA 03/10/2023
MEDTRONIC PUERTO RICO OPERATIONS CO. ENTERRA 05/13/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. ENTERRA 03/18/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. ENTERRA 12/07/2020
MEDTRONIC PUERTO RICO OPERATIONS CO. ENTERRA 08/05/2020
MEDTRONIC PUERTO RICO OPERATIONS CO. ENTERRA 09/24/2018
MEDTRONIC PUERTO RICO OPERATIONS CO. ENTERRA 01/12/2018
MEDTRONIC NEUROMODULATION ENTERRA 01/24/2017
MEDTRONIC PUERTO RICO OPERATIONS CO. ENTERRA 03/03/2016
MEDTRONIC PUERTO RICO OPERATIONS CO. ENTERRA 10/20/2014
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