• 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
 

 
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
113 records meeting your search criteria returned- Product Code: HSX Report Date From: 1/1/2017 Report Date To: 12/31/2017

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS, INC. UNKNOWN SROM DEPUY FEMUR 06/29/2017
SMITH & NEPHEW, INC. ARTICULAR SURFACE SIZE 5 8MM 06/28/2017
DEPUY ORTHOPAEDICS, INC. UNKNOWN LCS COMP RP INSERT STD+ 15MM 06/27/2017
MAKO SURGICAL CORP. UNKNOWN_RECONSTRUCTIVE_PRODUCT 06/26/2017
ZIMMER, INC. ZUK UNIVERAL HIGH FLEX PRECOAT FEMORAL C 06/22/2017
CONFORMIS, INC. IUNI G2 06/21/2017
SMITH & NEPHEW, INC. JOURNEY UNI TIB BASE LM/RL SZ 3 06/15/2017
AESCULAP IMPLANT SYSTEMS COLUMBUS RP TIBIAL PLATEAU CEMENTED T1 06/02/2017
ZIMMER, INC. ZIMMER UNICOMPARTMENTAL TIBIAL COMPONENT 06/01/2017
ZIMMER, INC. ZIMMER UNICOMPARTMENTAL ARTICULAR SURFAC 06/01/2017
-
-