• 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
 

 
 
6 records meeting your search criteria returned- Product Code: OQG Product Problem: Loosening of Implant Not Related to Bone-Ingrowth Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
AESCULAP AG VITELENE INSERT I 32MM POST.WALL 08/08/2023
BIOMET UK LTD. E1 TAPERED STD +3MM LNR 32/39 07/11/2023
BIOMET UK LTD. CER BIOLOXD OPTION HD 40MM 05/13/2021
AESCULAP AG PLASMAFIT POLY PFANNE GR.48MM F 12/10/2020
AESCULAP AG VITELENE INSERT G 36MM SYM. 08/20/2019
BIOMET FRANCE S.A.R.L. GTS STANDARD FMRL STEM SIZE -1 07/21/2019
-
-