Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
500 records meeting your search criteria returned. The results are incomplete - please narrow your search.

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US APG+ SIZER PIN GUIDE 52+0 12/14/2017
DEPUY ORTHOPAEDICS, INC. 1818910 APG+ SIZER PIN GUIDE 48+0 12/14/2017
DEPUY ORTHOPAEDICS, INC. 1818910 PFC*CALIBRATED PAT CUT GDE 12/14/2017
AESCULAP IMPLANT SYSTEMS VEGA PS REMOVABLE TRIAL FEMUR BOX F5 12/13/2017
ZIMMER BIOMET, INC. EXTENDED TIBIA JIG COMPLETE 12/13/2017
DEPUY INTERNATIONAL LTD. 8010379 SIGMA HP ADJ TIBIAL STYLUS 12/13/2017
DEPUY ORTHOPAEDICS INC US PFC*CALIBRATED PAT CUT GDE 12/13/2017
ZIMMER BIOMET, INC. FEMORAL HEAD PROVISIONAL 12/14 NECK TAPE 12/11/2017
DEPUY IRELAND 9616671 ATTUNE SHIM SZ5 5MM 12/11/2017
ZIMMER BIOMET, INC. NEXGEN ARTICULAR SURFACE PROVISIONAL 12/11/2017
-
-