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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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296 records meeting your search criteria returned- Product Code: OUR Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
SI-BONE, INC. IFUSE IMPLANT SYSTEM 05/20/2022
Unknown Manufacturer SI POSTERIOR ALLOGRAFT 04/26/2022
MEDTRONIC SOFAMOR DANEK USA, INC RIALTO SI FUSION SYSTEM 04/20/2022
SI-BONE, INC. IFUSE IMPLANT SYSTEM 01/12/2022
SI-BONE, INC. IFUSE IMPLANT SYSTEM 12/08/2021
SI-BONE, INC. IFUSE IMPLANT SYSTEM 12/01/2021
SI-BONE, INC. IFUSE IMPLANT SYSTEM 11/30/2021
SI-BONE, INC. IFUSE IMPLANT SYSTEM 11/23/2021
SI-BONE, INC. IFUSE IMPLANT SYSTEM 11/23/2021
SI-BONE, INC. IFUSE IMPLANT SYSTEM 11/11/2021
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