• 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 
 5 
 > 
 
50 records meeting your search criteria returned- Product Code: KWL Patient Problem: Osteolysis Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITH & NEPHEW ORTHOPAEDICS LTD HEMI HEAD 46MM 06/10/2022
SMITH & NEPHEW ORTHOPAEDICS LTD HEMI HEAD 48MM 05/19/2022
SMITH & NEPHEW ORTHOPAEDICS LTD HEMI HEAD 50MM 12/28/2021
ZIMMER BIOMET, INC. UNKNOWN CUP 11/17/2021
SMITH & NEPHEW ORTHOPAEDICS LTD HEMI HEAD 46MM 10/15/2021
SMITH & NEPHEW ORTHOPAEDICS LTD HEMI HEAD 42MM 09/29/2021
SMITH & NEPHEW ORTHOPAEDICS LTD HEMI HEAD 42MM 08/19/2021
SMITH & NEPHEW ORTHOPAEDICS LTD HEMI HEAD 46MM 05/27/2021
DEPUY ORTHOPAEDICS INC US P.F.C.*NONPOROUS STEM #5 12/09/2020
SMITH & NEPHEW ORTHOPAEDICS LTD HEMI HEAD 46MM 06/19/2020
-
-