• 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 
 > 
 
107 records meeting your search criteria returned- Product Code: LPH Product Problem: Patient Device Interaction Problem Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. UNKNOWN BIMETRIC STEM 11/08/2022
ZIMMER BIOMET, INC. UNKNOW MAGNUM PF CUP 11/08/2022
ZIMMER BIOMET, INC. 48MM O.D. SIZE GG POROUS UNCEMENTED WITH 11/04/2022
ZIMMER BIOMET, INC. UNKNOWN HEAD 11/04/2022
ZIMMER BIOMET, INC. UNKNOWN STEM 11/03/2022
ZIMMER BIOMET, INC. M2A-MAGNUM PF CUP 56ODX50ID 11/02/2022
LIMACORPORATE S.P.A. FEM. MODULAR HEAD - M Ø28MM 2 10/21/2022
ZIMMER BIOMET, INC. TAPERLOC POR FMRL 5.0X130 10/06/2022
LIMACORPORATE S.P.A. DELTA-TT ACETAB.CUP Ø52 MM 09/16/2022
BIOMET UK LTD. UNKNOWN BIOLOX DELTA HEAD 09/14/2022
-
-