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 
 > 
 
14 records meeting your search criteria returned- Product Code: KWA Product Problem: Entrapment of Device Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOMET ORTHOPEDICS, LLC ARCOS MODULAR REVISION SYSTEM 08/19/2020
DEPUY INTERNATIONAL LTD - 8010379 CHARN PIN RETRACT+HANLESET 03/18/2020
DEPUY ORTHOPAEDICS INC US UNK FEMORAL TRIAL 01/21/2020
JOHNSON AND JOHNSON/DEPUY PINNACLE 06/08/2017
BIOMET ORTHOPEDICS UNKNOWN CONSTRAINED LINER 02/08/2017
BIOMET ORTHOPEDICS M2A-MAGNUM ACETABULAR CUP 56MM OUTER DIA 09/28/2016
BIOMET UK LTD. EXCEED ABT RINGLOC-X SHELL PC DIA50MM 01/13/2016
BIOMET ORTHOPEDICS UNKNOWN HIP 09/09/2015
BIOMET ORTHOPEDICS ARCOS CON SZ B STD 70MM 04/23/2015
BIOMET ORTHOPEDICS UNKNOWN M2A 38 HEAD 09/02/2014
-
-