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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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177 records meeting your search criteria returned- Product Code: OXF Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
ALLERGAN / SOFREGEN MEDICAL INC. SERI SCAFFOLD MESH 05/10/2021
SOFREGEN MEDICAL SERI SCAFFOLD 04/21/2021
W. L. GORE & ASSOCIATES, INC. GORE® ENFORM INTRAPERITONEAL BIOMATERIAL 04/14/2021
ALLERGAN (MEDFORD) UNK SCAFFOLD 02/20/2017
ALLERGAN (MEDFORD) SERISCAFFOLD SURGICAL SCAFFOLD (OUS) 12/15/2016
ALLERGAN (MEDFORD) SERI SURGICAL SCAFFOLD (US) 09/07/2016
ALLERGAN (MEDFORD) SERI SURGICAL SCAFFOLD (US) 09/07/2016
ALLERGAN (MEDFORD) SERI SURGICAL SCAFFOLD (US) 08/25/2016
ALLERGAN SERI SURGICAL SCAFFOLDING 07/26/2016
ALLERGAN (MEDFORD) UNK SERI SURGICAL SCAFFOLD 05/18/2016
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