• 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 
 > 
 
57 records meeting your search criteria returned- Product Code: HWC Product Problem: Inadequacy of Device Shape and/or Size Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
EXTREMITY MEDICAL, LLC. CARPALFIX 03/12/2019
DEPUY MITEK LLC US MICRO QA+ #3/0 OC V4 W/BIT 01/11/2019
DEPUY MITEK LLC US MICRO QA+ #3/0 OC V4 W/BIT 01/11/2019
SMITH & NEPHEW, INC. UNKNOWN TRAUMA IMPLANT 11/27/2018
STRYKER GMBH ASNIS III CANNULATED TITANIUM SCREW, 8MM 10/31/2018
STRYKER GMBH ASNIS III CANNULATED TITANIUM SCREW, 8MM 10/31/2018
ZIMMER BIOMET, INC. UNKNOWN SCREW 08/29/2018
SMITH & NEPHEW, INC. BIOSURE HA 6MM X 25MM 06/24/2018
SMITH & NEPHEW, INC. BIOSURE HA 9MM X 30MM 06/12/2018
BIOMET MICROFIXATION 2.7X10MM HT X-DRIVE SCREW 12/13/2017
-
-