• 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 
 > 
 
64 records meeting your search criteria returned- Product Code: KIH Patient Problem: No Clinical Signs, Symptoms or Conditions Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY SPINE INC FEN OPEN CANNULA STRL 06/30/2022
WARSAW ORTHOPEDICS VOYAGER FENESTRATED SCREWS 06/24/2022
WARSAW ORTHOPEDICS VOYAGER FENESTRATED SCREWS 06/24/2022
MEDTRONIC SOFAMOR DANEK USA, INC VOYAGER FENESTRATED SCREWS 06/24/2022
WARSAW ORTHOPEDICS VOYAGER FENESTRATED SCREWS 06/03/2022
DEPUY ORTHOPAEDICS INC US SMARTMIX CEMVAC SYRINGE 06/02/2022
WARSAW ORTHOPEDICS VOYAGER FENESTRATED SCREWS 05/23/2022
WARSAW ORTHOPEDICS VOYAGER FENESTRATED SCREWS 05/23/2022
SYNTHES GMBH TRAUMACEM(TM) V+ SYRINGE KIT - STERILE 04/01/2022
WARSAW ORTHOPEDICS CD HORIZON® FENESTRATED SCREW SET 02/07/2022
-
-