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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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72 records meeting your search criteria returned- Product Code: EZX Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
MEDOS INTERNATIONAL SàRL CH UNKNOWN VERTEBRAL BODY REPLACEMENT - MES 09/28/2023
SYNTHES GMBH UNK - VERTEBRAL BODY REPLACEMENT - MESH: 06/05/2023
SYNTHES GMBH UNK - RESORBABLE IMPLANTS: MESH 03/27/2023
SYNTHES GMBH UNK - RESORBABLE IMPLANTS: MESH 03/27/2023
SYNTHES GMBH UNK - VERTEBRAL BODY REPLACEMENT - MESH: 12/27/2022
SYNTHES GMBH UNK - VERTEBRAL BODY REPLACEMENT - MESH: 10/05/2022
MEDTRONIC SOFAMOR DANEK USA, INC PYRAMESH TITANIUM MESH 04/27/2022
SYNTHES GMBH UNK - VERTEBRAL BODY REPLACEMENT - MESH: 11/02/2021
SYNTHES GMBH UNK - VERTEBRAL BODY REPLACEMENT - MESH: 11/02/2021
WRIGHTS LANE SYNTHES USA PRODUCTS LLC UNK - VERTEBRAL BODY REPLACEMENT - MESH: 10/28/2021
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