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 
 > 
 
27 records meeting your search criteria returned- Product Code: HWC Product Problem: Inadequacy of Device Shape and/or Size Report Date From: 01/1/2018
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ACUMED LLC 27.0MM ACUTRAK® FUSION DEVICE 12/10/2021
GRAHAM MEDICAL TECHNOLOGIES, LLC. DBA GR HYPROCURE 05/19/2021
GRAHAM MEDICAL TECHNOLOGIES, LLC. DBA GR HYPROCURE 05/19/2021
ZIMMER BIOMET, INC. UNKNOWN ZNN LOCKING SCREWS 03/26/2021
ZIMMER BIOMET, INC. UNKNOWN ZNN LOCKING SCREWS 03/26/2021
SKELETAL DYNAMICS SKELETAL DYNAMICS 03/10/2021
EXTREMITY MEDICAL XMCP 02/10/2021
STRYKER TRAUMA KIEL UNKNOWN LAG SCREW 01/04/2021
STRYKER TRAUMA KIEL UNKNOWN LAG SCREW CASE 1 01/04/2021
STRYKER TRAUMA KIEL UNKNOWN LAG SCREW CASE 3 01/04/2021
-
-