• 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
 

 
 < 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 > 
 
140 records meeting your search criteria returned- Product Code: PBI Patient Problem: Joint Dislocation Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOMET ORTHOPEDICS G7 NEUTRAL E1 LINER 32MM D 08/04/2017
BIOMET ORTHOPEDICS G7 NEUTRAL E1 LINER 32MM G 07/26/2017
BIOMET ORTHOPEDICS G7 NEUTRAL E1 LINER 32MM G 07/26/2017
BIOMET ORTHOPEDICS G7 NEUTRAL E1 LINER 32MM F 07/24/2017
BIOMET ORTHOPEDICS G7 SCREW 6.5MM X 20MM 06/06/2017
BIOMET ORTHOPEDICS G7 SCREW 6.5MM X 20MM 06/06/2017
BIOMET ORTHOPEDICS G7 SCREW 6.5MM X 25MM 06/06/2017
BIOMET ORTHOPEDICS G7 SCREW 6.5MM X 20MM 06/06/2017
BIOMET ORTHOPEDICS G7 ACETABULAR SYSTEM 04/14/2017
BIOMET ORTHOPEDICS G7 NEUTRAL E1 LINER 03/23/2017
-
-