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

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
 

 
 < 
 1 
 2 
 
 
17 records meeting your search criteria returned- Product Code: KWA Product Problem: Delivered as Unsterile Product Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. ARCOS 20X250MM CYL DIST 06/05/2019
ZIMMER BIOMET, INC. ARCOS 17X200MM CYL DIST 06/05/2019
ZIMMER BIOMET, INC. TPRLC 133 MP TYPE1 PPS SO 20.0 05/15/2019
ZIMMER BIOMET, INC. R/B RLOC LHOLE SHL 48MM SZ22 05/08/2019
ZIMMER BIOMET, INC. ECHO HIP FX LAT FEMORAL 15MM 04/29/2019
ZIMMER BIOMET, INC. TPRLC 133 MP T1 PPS SO 02/13/2019
ZIMMER BIOMET, INC. TPRLC 133 T1 PPS HO 02/11/2019
-
-