Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience
  • Print
  • Share
  • E-mail
-
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
 

 
 
 1 
 2 
 3 
 4 
 5 
 > 
 
49 records meeting your search criteria returned- Product Code: KWQ Product Problem: Patient Device Interaction Problem Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
NUVASIVE INC NUVASIVE ACP SYSTEM 03/06/2024
SYNTHES GMBH 4.0MM TI CERV SELF-RETAIN SCR SLF-DRLG/V 12/08/2023
SYNTHES GMBH 4.0MM TI CERV SELF-RETAIN SCR SLF-DRLG/V 12/08/2023
SYNTHES GMBH 4.0MM TI CERV SELF-RETAIN SCR SLF-DRLG/V 12/08/2023
SYNTHES GMBH 4.0MM TI CERV SELF-RETAIN SCR SLF-DRLG/V 12/08/2023
SYNTHES GMBH TI VECTRA(TM) PLATE 2 LEVEL/38MM 12/08/2023
SYNTHES GMBH VECTRA-T-PL 4/4.5 4 SEGMENTS L69 TAN 10/17/2023
SYNTHES GMBH 4.0MM TI CERV SELF-RETAIN SCR SLF-DRLG/V 10/10/2023
AESCULAP AG COLLECT.NO.QAS SPINE ANTERIOR STABILIS. 05/04/2023
AESCULAP AG COLLECT.NO.QAS SPINE ANTERIOR STABILIS. 05/04/2023
-
-