• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

  • 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 
 6 
 7 
 8 
 9 
 10 
 > 
 
130 records meeting your search criteria returned- Product Code: LGW Product Problem: Detachment of Device or Device Component Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
NEVRO CORP. SENZA 03/05/2020
NEVRO CORP. SENZA 03/03/2020
NEVRO CORP. SENZA 02/21/2020
NEVRO CORP. SENZA 02/07/2020
NEVRO CORP. SENZA 02/03/2020
BOSTON SCIENTIFIC NEUROMODULATION PRECISION 11/12/2019
NEVRO CORP. SENZA 09/11/2019
NUVECTRA CORPORATION NUVECTRA CORPORATION 08/27/2019
NEVRO CORP. SENZA 08/26/2019
NEVRO CORP. SENZA 08/16/2019
-
-