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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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156 records meeting your search criteria returned- Product Code: GXN Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
SYNTHES GMBH PSI SD800.439 PEEK IMPLANT 08/24/2022
SYNTHES GMBH PSI SD800.435 PEEK IMPLANT 08/24/2022
SYNTHES GMBH PSI SD800.441 PEEK IMPLANT 08/11/2022
WRIGHTS LANE SYNTHES USA PRODUCTS LLC PSI SD800.440 PEEK IMPLANT 08/04/2022
SYNTHES GMBH PSI 140*140*40 PEEK 07/29/2022
SYNTHES GMBH PSI 140*100*40 PEEK 07/22/2022
WRIGHTS LANE SYNTHES USA PRODUCTS LLC PSI SD800.434 PEEK IMPLANT 06/30/2022
OXFORD PERFORMANCE MATERIALS, INC. HTR-PEKK 05/23/2022
OXFORD PERFORMANCE MATERIALS, INC. HTR-PEKK 05/20/2022
WRIGHTS LANE SYNTHES USA PRODUCTS LLC PSI SD800.540 PEEK IMPLANT 05/04/2022
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