• 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 
 > 
 
77 records meeting your search criteria returned- Product Code: LKF Patient Problem: Insufficient Information Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
COOPERSURGICAL, INC. RUMI II,BACKLOADABLE 10/05/2021
CONMED CORPORATION VCARE-MEDIUM 10/01/2021
CONMED CORPORATION VCARE 09/24/2021
Unknown Manufacturer UTERINE MANIPULATOR 09/14/2021
CONMED CORPORATION VCARE 09/07/2021
CONMED UTICA VCARE - SMALL 08/30/2021
COOK / COOK INCORPORATED COOK UTERINE BALLOON 08/30/2021
CONMED UTICA VCARE 200A - SMALL 08/30/2021
CONMED CORPORATION VCARE MEDIUM UTERINE MANIPULATOR 08/27/2021
CONMED CORPORATION VCARE 08/26/2021
-
-