• 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 
 6 
 7 
 8 
 9 
 10 
 > 
 
123 records meeting your search criteria returned- Product Code: NTG Product Problem: Insufficient Information Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
STRYKER GMBH SCANDINAVIAN TOTAL ANKLE REPLACEMENT 04/19/2021
ZIMMER BIOMET, INC. UNKNOWN ARTICULAR SURFACE 08/03/2020
STRYKER GMBH SLIDING CORE UHMPWE, 6MM 10/25/2018
STRYKER GMBH SLIDING CORE UHMPWE, 7MM 10/25/2018
STRYKER GMBH TALAR COMP,SINGLE COATED US VERSION SMAL 10/25/2018
STRYKER GMBH UNKNOWN STAR ANKLE 10/19/2018
STRYKER GMBH UNKNOWN STAR TIBIA 04/17/2018
STRYKER GMBH UNKNOWN STAR TALAR 04/17/2018
ZIMMER BIOMET, INC. UNKNOWN TIBIAL COMPONENT 03/29/2018
STRYKER GMBH TIBIAL COMP,SINGLECOATED US VERSION, LAR 03/28/2018
-
-