• 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
 

 
 
8 records meeting your search criteria returned- Product Code: MRA Patient Problem: Adhesion(s) Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US SROM*STM ST,36+8L NK,20X15X165 02/01/2024
DEPUY ORTHOPAEDICS INC US PINNACLE MTL INS NEUT36IDX54OD 07/27/2023
DEPUY ORTHOPAEDICS INC US UNK HIP ACETABULAR LINER METAL PINNACLE 05/23/2023
DEPUY ORTHOPAEDICS INC US PINNACLE MTL INS NEUT28IDX50OD 03/10/2023
DEPUY ORTHOPAEDICS INC US PINNACLE SECTOR II CUP 60MM 04/01/2021
DEPUY ORTHOPAEDICS INC US PINN MAR LIP LNR 28IDX56OD 06/12/2020
DEPUY ORTHOPAEDICS INC US MBT CEM KEEL TIB TRAY SZ4 12/19/2019
DEPUY ORTHOPAEDICS INC US PINNACLE SECTOR II CUP 50MM 10/10/2019
-
-