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

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
JOHNSON AND JOHNSON DEPUY AML 03/20/2014
JOHNSON AND JOHNSON DEPUY DURALOC CUP 03/20/2014
1818910 DEPUY ORTHOPAEDICS, INC. SOL SYS 8/12.0 LRG ST 03/20/2014
BIOMET ORTHOPEDICS TAPERLOC POR LAT FMRL 9X137 03/19/2014
BIOMET ORTHOPEDICS INTEGRAL/X POR STANDARD 9MM 03/19/2014
BIOMET ORTHOPEDICS RNGLC LOCKING RING SZ 23 03/18/2014
BIOMET ORTHOPEDICS TAPERLOC POR LAT FMRL 9X137 03/13/2014
BIOMET ORTHOPEDICS TAPERLOC POR RED/LAT 12.5X145 03/13/2014
BIOMET ORTHOPEDICS TAPERLOC POR FMRL 9X137 03/11/2014
BIOMET ORTHOPEDICS MLRY-HD POR FMRL 11X160MM 03/10/2014
-
-