• 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 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
135 records meeting your search criteria returned- Product Code: MRA Report Date From: 1/1/2023 Report Date To: 12/31/2023

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US SROM*STM ST,36+8L NK,20X15X165 07/27/2023
DEPUY ORTHOPAEDICS INC US PINNACLE MTL INS NEUT36IDX54OD 07/27/2023
DEPUY ORTHOPAEDICS INC US SROM*STM ST,36+8L NK,18X13X160 07/27/2023
DEPUY ORTHOPAEDICS INC US SROM*STM ST,36+8L NK,20X15X165 07/26/2023
ZIMMER SWITZERLAND MANUFACTURING GMBH DURASUL®, ALPHA INSERT, II/36 07/24/2023
DEPUY ORTHOPAEDICS INC US DELTA CER INSERT 32ID X 52OD 07/20/2023
DEPUY ORTHOPAEDICS INC US DELTA CER INSERT 28ID X 52OD 07/14/2023
DEPUY ORTHOPAEDICS INC US DELTA CER INSERT 32ID X 48OD 07/13/2023
SMITH & NEPHEW, INC. R3 3 HOLE ACET SHELL MM48 07/11/2023
DEPUY ORTHOPAEDICS INC US DELTA CER INSERT 36ID X 56OD 07/10/2023
-
-