• 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 
 > 
 
289 records meeting your search criteria returned- Product Code: HWT Patient Problem: No Known Impact Or Consequence To Patient Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. OXFORD FEMORAL DRILL GUIDE LATERAL IM AD 01/26/2021
ZIMMER BIOMET, INC. PROVISIONAL STEMMED TIBIAL COMPONENT SIZ 12/30/2020
ZIMMER BIOMET, INC. ARTICULAR SURFACE PROVISIONAL SIZE GH 10 11/12/2020
SMITH & NEPHEW, INC. ARTICULAR SURFACE PROVISIONAL SZ 5 8MM 10/19/2020
ZIMMER BIOMET, INC. BMT TIB LOCKING TRL 67MM 10/16/2020
ZIMMER BIOMET, INC. PROVISIONAL ARTICULAR SURFACE SIZE STRIP 10/15/2020
SMITH & NEPHEW, INC. MODIFIED JII TIBIA CUTTING BLOCK RIGHT 09/30/2020
ZIMMER BIOMET, INC. ARTICULAR SURFACE PROVISIONAL SIZE EF 10 09/01/2020
ZIMMER BIOMET, INC. NEXGEN TIBIAL ARTICULAR SURFACE PROVISIO 08/28/2020
ZIMMER BIOMET, INC. NEXGEN STEMMED TIBIAL COMPONENT PROVISIO 08/28/2020
-
-