• 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
ENCORE MEDICAL L.P EMPOWR PS KNEE 03/02/2021
ZIMMER BIOMET, INC. UNK FEMORAL COMPONENT 02/12/2021
ZIMMER BIOMET, INC. ARTICULAR SURFACE WITH LOCKING SCREW SIZ 02/01/2021
ZIMMER BIOMET, INC. FLEX ARTICULAR SURFACE LOCKING SCREW 02/01/2021
ZIMMER BIOMET, INC. UNKNOWN BIOMET 360 TIBIAL AUGMENT 01/23/2021
ZIMMER BIOMET, INC. UNKNOWN PERSONA FEMORAL PROVISIONAL 01/22/2021
ZIMMER MANUFACTURING B.V. STEMMED TIBIAL COMPONENT PRECOAT SIZE 7 01/12/2021
ZIMMER BIOMET, INC. UNKNOWN OSS TIBIAL INSERT 01/08/2021
ZIMMER BIOMET, INC. UNKNOWN OSS FEMORAL 01/08/2021
ZIMMER BIOMET, INC. UNKNOWN 11X190MM CEMENTED STEM 01/07/2021
-
-