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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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4 records meeting your search criteria returned- Product Code: LOE Patient Problem: No Information Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
EBI, LLC. SPF-PLUS 60/M 06/30/2020
EBI, LLC. EBI SPF-XL IIB 2/DM IMPLANTABLE SPINAL F 06/28/2018
EBI, LLC. OSTEOGEN-40/M 06/21/2018
EBI, LLC. SPF-XL IIB 2/DM 01/11/2018
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