• 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 
 > 
 
12 records meeting your search criteria returned- Product Code: KWY Patient Problem: Bacterial Infection Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITH & NEPHEW ORTHOPAEDICS AG UNKN. SL-PLUS FAMILY STEM (UNKN. SUB-FAM 06/14/2021
SMITH & NEPHEW, INC. TANDEM BIPOLAR COCR 55OD 28ID 05/06/2021
ZIMMER BIOMET, INC. BIOMET UNKNOWN E1 MAXROM LINER 08/08/2018
ZIMMER BIOMET, INC. BIOMET UNKNOWN MH RINGLOC SHELL 08/08/2018
ZIMMER BIOMET, INC. BIOMET UNKNOWN SHELL 08/07/2018
ZIMMER BIOMET, INC. BIOMET UNKNOWN HEAD 08/07/2018
ZIMMER BIOMET, INC. BIOMET UNKNOWN TAPERLOC STEM 08/07/2018
ZIMMER BIOMET, INC. BIOMET UNKNOWN SHELL 08/07/2018
ZIMMER BIOMET, INC. BIOMET UNKNOWN TAPERLOC STEM 08/07/2018
ZIMMER BIOMET, INC. BIOMET UNKNOWN SHELL 08/03/2018
-
-