• 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
 

 
 < 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 > 
 
161 records meeting your search criteria returned- Product Code: HRY Report Date From: 1/1/2024 Report Date To: 12/31/2024

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. VNGD CR TIB BRG 18X79/83 02/05/2024
DEPUY ORTHOPAEDICS INC US ENDURON 10D 54OD X 28ID 02/05/2024
SMITH & NEPHEW, INC. GII UNIVERSAL EXTRACTOR 02/02/2024
SMITH & NEPHEW, INC. FEMORAL HEAD IMPACTOR 02/02/2024
SMITH & NEPHEW, INC. GII ARTICULAR INSERTER/EXTRACT 01/31/2024
SMITH & NEPHEW, INC. GII UNIVERSAL EXTRACTOR 01/31/2024
SMITH & NEPHEW, INC. R3 OFFSET IMPACTOR TIP 01/31/2024
MICROPORT ORTHOPEDICS INC. ADVANCE® II COCR TIBIAL BASE NONPOROUS 01/27/2024
MICROPORT ORTHOPEDICS INC. ADVANCE® II COCR TIBIAL BASE NONPOROUS 01/27/2024
MICROPORT ORTHOPEDICS INC. ADVANCE® II COCR TIBIAL BASE NONPOROUS 01/27/2024
-
-