• 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 
 > 
 
24 records meeting your search criteria returned- Product Code: HRY Product Problem: Material Integrity Problem Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOMET UK LTD. OXF TRIAL BEARING MED SZ 4/5 03/12/2021
BIOMET UK LTD. OXF TRIAL BEARING MED SZ 4/5 02/24/2021
SMITH & NEPHEW, INC. JOURNEY LOCK FEM IMPL IMPACT 02/11/2021
SMITH & NEPHEW, INC. JOURNEY LOCK FEM IMPL IMPACT 02/09/2021
BIOMET UK LTD. OXF TRL BRG W/SLOTS MED 3MM MM 12/15/2020
AESCULAP AG AS UNIVATION XF FEMUR CEMENTED F3 RM 02/21/2019
STRYKER ORTHOPAEDICS-MAHWAH TRIATHLON PKR INSERT X3 #2 RM/LL -8MM 04/19/2017
STRYKER ORTHOPAEDICS-MAHWAH TRIATHLON PKR INSERT X3 #2 LM/RL -9MM 11/20/2016
STRYKER ORTHOPAEDICS-MAHWAH TRIATHLON PKR INSERT X3 #3 LM/RL -8MM 07/12/2016
STRYKER ORTHOPAEDICS-MAHWAH TRIATHLON PKR INSERT X3 #2 LM/RL -8MM 11/08/2015
-
-