• 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 
 3 
 4 
 > 
 
36 records meeting your search criteria returned- Product Code: LOD Patient Problem: Necrosis Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SYNTHES GMBH UNK - BIOMATERIAL - CEMENT: TRAUMACEM 04/18/2024
SYNTHES GMBH UNK - BIOMATERIAL - CEMENT 08/11/2023
SYNTHES GMBH TRAUMACEM(TM) V+ INJECTABLE BONE CEMENT 06/16/2023
ZIMMER BIOMET, INC. UNKNOWN PLACOS BONE CEMENT 05/15/2023
DEPUY ORTHOPAEDICS INC US DEPUY CMW 2 20G 08/12/2022
SYNTHES GMBH UNK - BIOMATERIAL - CEMENT: TRAUMACEM 06/27/2022
SYNTHES GMBH TRAUMACEM(TM) V+ INJECTABLE BONE CEMENT 06/27/2022
BIOMET FRANCE S.A.R.L. BIOMET BONE CEMENT R 1X40 US 06/01/2022
BIOMET FRANCE S.A.R.L. BIOMET BONE CEMENT R 1X40 US 06/01/2022
DEPUY ORTHOPAEDICS INC US DEPUY CMW 1 40G 03/19/2022
-
-