• 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 
 > 
 
392 records meeting your search criteria returned- Product Code: LPH Product Problem: Loosening of Implant Not Related to Bone-Ingrowth Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. G7 OSSEOTI 4 HOLE SHELL 60MM G 02/20/2024
SMITH & NEPHEW ORTHOPAEDICS AG UNKNOWN POLARCUP PLASTIC INSERT 02/20/2024
AESCULAP AG ISODUR PROSTHESIS HEAD 12/14 22.2MM M 02/07/2024
SMITH & NEPHEW, INC. COCR 12/14 FEM HEAD 26 + 0 01/30/2024
ZIMMER BIOMET, INC. M2A-MAGNUM 42-50MM TPR INSRT-6 01/30/2024
ZIMMER BIOMET, INC. M2A-MAGNUM PF CUP 48ODX42ID 01/30/2024
SMITH & NEPHEW, INC. UNKNOWN REFLECTION ALL-POLY CUP 01/24/2024
SMITH & NEPHEW, INC. UNKNOWN REFLECTION ALL-POLY CUP 01/24/2024
SMITH & NEPHEW, INC. UNKNOWN REFLECTION ALL-POLY CUP 01/24/2024
SMITH & NEPHEW, INC. UNKNOWN REFLECTION ALL-POLY CUP 01/22/2024
-
-