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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
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303 records meeting your search criteria returned- Product Code: LOF Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
EBI, LLC. SPINALPAK ASSEMBLY 01/05/2023
EBI, LLC. ELECTRODE COVER PATCHES 12/15/2022
EBI, LLC. ORTHOPAK ASSEMBLY 12/02/2022
EBI, LLC. SOFT-TOUCH ELECTRODES, 72R 12/02/2022
EBI, LLC. SOFT-TOUCH ELECTRODES, 63B 11/04/2022
EBI, LLC. SOFT-TOUCH ELECTRODES, 63B 10/27/2022
EBI, LLC. SPINALPAK ASSEMBLY 10/18/2022
EBI, LLC. SOFT-TOUCH ELECTRODES, 63B 10/18/2022
EBI, LLC. BIOMET EBI BONE HEALING SYSTEM 10/10/2022
EBI, LLC. SFLX - XL COILETTE 10/10/2022
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