• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

  • 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 
 > 
 
16 records meeting your search criteria returned- Product Code: LWJ Product Problem: Noise, Audible Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MICROPORT ORTHOPEDICS INC. PROFEMUR® MODULAR FEMORAL NECK 11/01/2022
MICROPORT ORTHOPEDICS INC. PROFEMUR® MODULAR FEMORAL NECK 02/15/2022
AESCULAP IMPLANT SYSTEMS PLASMACUP FIXATION SCREW 6.5X20MM 08/17/2017
MICROPORT ORTHOPEDICS INC. PROFEMUR(R) MODULAR FEMORAL NECK 11/30/2016
MICROPORT ORTHOPEDICS INC. PROFEMUR(R) MODULAR FEMORAL NECK 11/18/2016
MICROPORT ORTHOPEDICS INC. PROFEMUR(R) MODULAR FEMORAL NECK 07/13/2015
MICROPORT ORTHOPEDICS INC. PROFEMUR(R) MODULAR FEMORAL NECK 06/04/2015
MICROPORT ORTHOPEDICS INC. PROFEMUR(R) MODULAR FEMORAL NECK 05/27/2015
MICROPORT ORTHOPEDICS INC. PROFEMUR(R) MODULAR FEMORAL NECK 04/29/2015
MICROPORT ORTHOPEDICS INC. PROFEMUR(R) MODULAR FEMORAL NECK 04/29/2015
-
-