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

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 
 > 
 
38 records meeting your search criteria returned- Product Code: MRA Patient Problem: Inflammation Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US DELTA CER INSERT 32ID X 50OD 02/22/2024
SMITH & NEPHEW, INC. R3 3 HOLE ACET SHELL 52MM 07/05/2023
BIOMET UK LTD. TAPERLOC BMPC 13.5X147MM 12/14 03/24/2023
SMITH & NEPHEW, INC. R3 32MM ID US CRMC LINER 50 12/07/2021
SMITH & NEPHEW, INC. SYN POR FEM COMP SZ 16 06/07/2021
DEPUY ORTHOPAEDICS INC US SUMMIT POR TAPER SZ2 STD OFF 08/26/2020
ZIMMER BIOMET, INC. BONE SCREW SELF-TAPPING 6.5 MM DIA. 30 M 12/07/2019
ZIMMER BIOMET, INC. BONE SCREW SELF-TAPPING 6.5 MM DIA. 35 M 12/07/2019
DEPUY ORTHOPAEDICS INC US SROM*STMLG36+21CR8L 20X15X225R 09/16/2019
DEPUY ORTHOPAEDICS INC US PINNACLE SECTOR II CUP 52MM 06/11/2019
-
-