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

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US SUMMIT POR TAPER SZ7 STD OFF 06/22/2017
DEPUY ORTHOPAEDICS, INC. 1818910 SUMMIT POR TAPER SZ2 HI OFF 02/07/2017
DEPUY ORTHOPAEDICS INC US SUMMIT DUOFIX TAP SZ6 HI OFF 11/15/2016
DEPUY ORTHOPAEDICS INC US SUMMIT POR TAPER SZ7 HI OFF 06/01/2016
DEPUY ORTHOPAEDIC INC, 1818910 S-ROM*STM STD,30 NK,16X11X150 05/31/2016
DEPUY ORTHOPAEDICS INC US ARTICULEZE M HEAD 36MM +12 02/16/2016
BIOMET ORTHOPEDICS TAPERLOC POR LAT FMRL 9X137 09/17/2015
BIOMET ORTHOPEDICS MLRY-HD LAT POR FMRL 10MM 09/02/2015
DEPUY ORTHOPAEDICS, INC. - 1818910 ALTRX +4 NEUT 40IDX56OD 07/02/2015
BIOMET ORTHOPEDICS TAPERLOC POR RED/LAT 17.5X155 05/06/2015
-
-