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 
 > 
 
26 records meeting your search criteria returned- Product Code: KNH Patient Problem: Unspecified Infection Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
Unknown Manufacturer FILSHIE CLIPS 08/25/2023
FEMCARE, LTD FILSHIE CLIP 08/12/2023
HOLOGIC, INC. ADIANA PERMANENT CONTRACEPTION SYSTEM 07/01/2022
HOLOGIC, INC. ADIANA 05/10/2022
FEMCARE - NIKOMED LTD FILSHIE CLIPS 11/19/2020
COOPERSURGICAL, INC/FEMCARE LTD. FILSHIE CLIP 08/05/2019
FEMCARE LTD. FILSHIE CLIPS 07/05/2019
COOPERSURGICAL, INC. FILSHIE CLIPS / CLAMPS 04/02/2019
Unknown Manufacturer FILSHIE CLIP 07/26/2018
COOPER SURGICAL FILSHIE CLIPS 09/26/2017
-
-