• 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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 > 
 
104 records meeting your search criteria returned- Product Code: HSX Patient Problem: Injury Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITH & NEPHEW, INC. JOURNEY UNI TIBINRT S5-6RM/LL9MM 10/16/2018
MAKO SURGICAL CORP. UNKNOWN MAKO LEFT MEDIAL FEMORAL COMPONE 09/27/2018
MAKO SURGICAL CORP. UNKNOWN MAKO LEFT MEDIAL BASEPLATE 09/27/2018
MAKO SURGICAL CORP. UNKNOWN MAKO LEFT MEDIAL POLY INSERT 09/27/2018
MAKO SURGICAL CORP. UNKNOWN MAKO BASEPLATE 08/31/2018
MAKO SURGICAL CORP. UNKNOWN MAKO FEMORAL COMPONENT 08/31/2018
SMITH & NEPHEW, INC. JRNY UNI TIBIAL BASE LM/RL SZ 6 08/24/2018
SMITH & NEPHEW, INC. JUNI OX FB FEM SZ 6 LM RL 08/23/2018
SMITH & NEPHEW, INC. JRNY UNI TIBIAL BASE LM/RL SZ 1 08/22/2018
SMITH & NEPHEW, INC. JRNY UNI TIBIAL BASE RM/LL SZ 5 06/27/2018
-
-