• 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
 

 
 
 1 
 2 
 3 
 > 
 
28 records meeting your search criteria returned- Product Code: MRA Patient Problem: Inflammation Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
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
SMITH & NEPHEW, INC. UNKNOWN CERAMIC BIOLOX DELTA LINER IMPLA 07/06/2020
SMITH & NEPHEW, INC. UNKNOWN CERAMIC BIOLOX DELTA FEMORAL HEA 07/06/2020
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
STRYKER ORTHOPAEDICS-MAHWAH TRIDENT ALUMINA INSERT 05/21/2019
-
-