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

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
 

 
 < 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 
 
101 records meeting your search criteria returned- Product Code: LKF Report Date From: 1/1/2022 Report Date To: 12/31/2022

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CONMED CORPORATION VCARE 02/14/2022
CONMED UTICA VCARE 200A - MEDIUM 02/10/2022
CONMED UTICA VCARE 200A - MEDIUM 02/10/2022
CONMED UTICA VCARE 200A - MEDIUM 02/10/2022
CONMED UTICA VCARE 200A - MEDIUM 02/10/2022
COOPERSURGICAL, INC. RUMI II,BACKLOADABLE 02/07/2022
COOPERSURGICAL, INC. RUMI II,BACKLOADABLE 02/04/2022
CLINICAL INNOVATIONS CLEARVIEW UTERINE MANIPULATOR 02/02/2022
CONMED UTICA VCARE 200A - MEDIUM 01/17/2022
COOPERSURGICAL, INC. UTERINE MANIPULATOR TIP L 01/16/2022
-
-