• 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 
 8 
 9 
 10 
 > 
 
204 records meeting your search criteria returned- Product Code: HWC Product Problem: Patient-Device Incompatibility Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
STRYKER HOWMEDICA OSTEONICS GROUP FIXING SCREW 04/13/2020
ARTHREX, INC. LOCKING SCREW, TITANIUM 3.5MM X 18MM 03/09/2020
ARTHREX, INC. LO-PRO SCRW,TI,3.5MMX 36MM 03/09/2020
ARTHREX, INC. LO-PRO SCRW,TI,3.5MMX 32MM 03/09/2020
BIOMET MICROFIXATION 2.4MM SYSTEM HIGH TORQUE (HT) CROSS-DRIV 03/02/2020
BIOMET MICROFIXATION 2.4MM SYSTEM HIGH TORQUE (HT) CROSS-DRIV 03/02/2020
BIOMET MICROFIXATION 2.4MM SYSTEM HIGH TORQUE (HT) CROSS-DRIV 01/03/2020
ARTHREX, INC. SUTR ANCH,CRKSCRW FT 12/26/2019
ARTHREX, INC. COMPR FT SCRW, 5.0 LG, 55MM LGTH 12/20/2019
ARTHREX, INC. COMPR FT SCRW, 7.0 XL, 70MM LGTH 12/20/2019
-
-