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

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
 

 
 
8 records meeting your search criteria returned- Product Code: HWT Product Problem: Inadequacy of Device Shape and/or Size Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. EXACT ALLIANCE BROACH/PROV14MM 02/16/2023
ZIMMER BIOMET, INC. PROVISIONAL STEMMED TIBIAL COMPONENT SIZ 10/06/2022
ZIMMER BIOMET, INC. UNKNOWN BROACH 07/01/2019
DEPUY ORTHOPAEDICS, INC. 1818910 LCS FEM GD POSITIONER 02/07/2019
DEPUY ORTHOPAEDICS, INC. 1818910 LCS FEM GD POSITIONER 02/07/2019
DEPUY ORTHOPAEDICS, INC. 1818910 LCS FEM GD POSITIONER 02/07/2019
SYNTHES SELZACH PATIENT SPECIFIC SPLINT ORTHOGNATHIC, IN 01/05/2017
SYNTHES SELZACH PATIENT SPECIFIC SPLINT ORTHOGNATHIC, FI 08/14/2015
-
-