• 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 
 > 
 
13 records meeting your search criteria returned- Product Code: MRA Product Problem: Inadequacy of Device Shape and/or Size Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITH & NEPHEW, INC. ANTHOLOGY SO POROUS SIZE 3 04/19/2023
DEPUY ORTHOPAEDICS INC US SUMMIT POR TAPER SZ10 HI OFF 03/23/2020
DEPUY ORTHOPAEDICS INC US PINNACLE SECTOR II CUP 50MM 12/02/2019
ZIMMER MANUFACTURING B.V. BONE SCR 6.5X20 SELF-TAP 11/19/2018
ZIMMER MANUFACTURING B.V. BONE SCR 6.5X30 SELF-TAP 08/29/2018
DEPUY IRELAND 9616671 S-ROM*SLEEVE PRX ZTT, 16F-SML 05/24/2017
DEPUY IRELAND 9616671 SROM STM ST,36+6L NK,11X16X150 05/24/2017
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN TRIDENT SHELL 05/17/2017
STRYKER ORTHOPAEDICS-MAHWAH TRIDENT ALUMINA INSERT 02/22/2016
DEPUY ORTHOPAEDICS, INC. TRI-LOCK BPS SZ 5 HI OFFSET 01/22/2015
-
-