• 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 
 > 
 
26 records meeting your search criteria returned- Product Code: MRA Patient Problem: Limited Mobility Of The Implanted Joint Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US EA DELTA CER INSERT 36IDX52OD 09/11/2020
DEPUY ORTHOPAEDICS INC US EA DELTA CER INSERT 36IDX54OD 08/03/2020
DEPUY ORTHOPAEDICS INC US DELTA CER HEAD 12/14 36MM +8.5 04/03/2020
DEPUY ORTHOPAEDICS INC US SUMMIT POR TAPER SZ10 HI OFF 03/23/2020
DEPUY ORTHOPAEDICS INC US SROM STM STD 36+12L 15X20 03/11/2020
DEPUY ORTHOPAEDICS INC US SROM STM STD 36+12L 13X18 03/05/2020
DEPUY ORTHOPAEDICS INC US SROM STM STD 36+12L 13X18 10/28/2019
DEPUY ORTHOPAEDICS INC US PINNACLE SECTOR II CUP 50MM 10/10/2019
DEPUY ORTHOPAEDICS INC US SROM STM ST,36+6L NK,11X16X150 09/24/2019
DEPUY ORTHOPAEDICS INC US PINNACLE MULTIHOLE II CUP 50MM 03/19/2019
-
-