• 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 
 4 
 > 
 
37 records meeting your search criteria returned- Product Code: KWY Patient Problem: Scar Tissue Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER MANUFACTURING B.V. SHELL 45 MM O.D. 08/22/2022
DEPUY ORTHOPAEDICS INC US SELF CENT HIP 42X28 RUST 04/25/2022
ZIMMER BIOMET, INC. ZB 12/14 COCR FRDM 36MM X +6 01/25/2022
ZIMMER BIOMET, INC. ZB 12/14 COCR FRDM 36MM X +6 12/01/2021
ZIMMER BIOMET, INC. UNKNOWN STEM 10/30/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL HEAD 03/17/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 03/17/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP ACETABULAR LINERS 03/17/2020
ZIMMER BIOMET, INC. M2A-MAGNUM PF CUP 52ODX46ID 01/21/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL HEAD 01/13/2020
-
-