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 
 > 
 
13 records meeting your search criteria returned- Product Code: LWJ Report Date From: 1/1/2024 Report Date To: 12/31/2024

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MICROPORT ORTHOPEDICS INC. PROFEMUR® MODULAR FEMORAL NECK 03/12/2024
MICROPORT ORTHOPEDICS INC. PROFEMUR® MODULAR FEMORAL NECK 03/05/2024
GLOBUS MEDICAL, INC. STELKAST HIP ARTHROPLASTY 03/05/2024
MICROPORT ORTHOPEDICS INC. PROFEMUR® MODULAR FEMORAL NECK 02/28/2024
MICROPORT ORTHOPEDICS INC. PROFEMUR® MODULAR FEMORAL NECK 02/27/2024
AESCULAP AG PLASMACUP MSC SIZE 58MM 02/23/2024
AESCULAP AG SC/MSC PE-INSERT 28MM 56/58 SYM. 02/23/2024
CORIN LTD TRINITY 02/22/2024
CORIN LTD (UK & FR) TRINITY 02/13/2024
MICROPORT ORTHOPEDICS INC. PROFEMUR® NECK 02/08/2024
-
-