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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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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
WRIGHTS LANE SYNTHES USA PRODUCTS LLC UNK - VERTEBRAL BODY REPLACEMENT - MESH: 10/28/2021
WRIGHTS LANE SYNTHES USA PRODUCTS LLC UNK - VERTEBRAL BODY REPLACEMENT - MESH: 10/28/2021
SYNTHES GMBH UNK - VERTEBRAL BODY REPLACEMENT - MESH: 10/11/2021
SYNTHES GMBH UNK - VERTEBRAL BODY REPLACEMENT - EXPAN 10/09/2021
SYNTHES GMBH UNK - VERTEBRAL BODY REPLACEMENT - EXPAN 10/09/2021
SYNTHES GMBH UNK - VERTEBRAL BODY REPLACEMENT - MESH: 10/08/2021
SYNTHES GMBH UNK - VERTEBRAL BODY REPLACEMENT - MESH 06/08/2021
SYNTHES GMBH UNK - RESORBABLE IMPLANTS: MESH 06/08/2021
MEDOS INTERNATIONAL SàRL CH UNKNOWN VERTEBRAL BODY REPLACEMENT - MES 06/07/2021
MEDOS INTERNATIONAL SàRL CH UNKNOWN VERTEBRAL BODY REPLACEMENT - MES 06/07/2021
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