• 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
 

 
 < 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 16 
 > 
 
168 records meeting your search criteria returned- Product Code: HWT Patient Problem: No Patient Involvement Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. NEXGEN STEMMED TIBIAL PROVISIONAL 06/01/2018
ZIMMER BIOMET, INC. NEXGEN STEMMED TIBIAL PROVISIONAL 06/01/2018
ZIMMER BIOMET, INC. ZIMMER UNICOMPARTMENTAL ARTICULAR SURFAC 05/25/2018
BIOMET UK LTD. OXF UNI I/M ROD LINK 05/23/2018
ZIMMER BIOMET, INC. NEXGEN LPS ARTICULAR SURFACE PROVISIONAL 03/23/2018
ZIMMER BIOMET, INC. PERSONA ARTICULAR SURFACE PROVISIONAL 11/13/2017
ZIMMER GMBH ANATOMICAL SHOULDER TRIAL HUMERAL PE-INS 10/12/2017
ZIMMER GMBH ANATOMICAL SHOULDER, TRIAL HUMERAL PE-IN 10/12/2017
ZIMMER GMBH ANATOMICAL SHOULDER, TRIAL HUMERAL PE-IN 09/06/2017
ZIMMER, INC. NEXGEN PROVISIONAL TIBIAL STEM 07/29/2017
-
-