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
 

 
 
7 records meeting your search criteria returned- Product Code: HDB Product Problem: Detachment of Device or Device Component Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CLINICAL INNOVATIONS, LLC KIWI OMNICUP 06/15/2023
CLINICAL INNOVATIONS, LLC. KIWI COMPLETE VACUUM DELIVERY SYSTEM 04/20/2023
CLINICAL INNOVATIONS, LLC KIWI 08/11/2022
CLINICAL INNOVATIONS KIWI VACUUM ASSISTED DELIVERY 07/21/2022
CLINICAL INNOVATIONS, LLC. KIWIPRO COMPLETE VACUUM DELIVERY SYSTEM 10/11/2019
CLINICAL INNOVATIONS, LLC KIWI® OMNICUP® 10/03/2019
CLINICAL INNOVATIONS, LLC KIWI COMPLETE VACUUM DELIVERY SYSTEM 09/23/2019
-
-