• 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 
 > 
 
28 records meeting your search criteria returned- Product Code: PHX Patient Problem: Nerve Damage Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. UNK INTERCALARY SEGMENT 11/07/2023
ZIMMER BIOMET, INC. UNK DISTAL HUMERAL COMPONENT 11/07/2023
ZIMMER BIOMET, INC. UNK PROXIMAL HUMERAL COMPONENT 11/07/2023
ZIMMER BIOMET, INC. UNKNOWN SRS 11/07/2023
ZIMMER BIOMET, INC. UNKNOWN COMPREHENSIVE HUMERAL STEM 09/20/2023
TORNIER S.A.S. TORNIER PERFORM REVERSED LATER ALIZED B 06/26/2023
TORNIER INC UNKNOWN TORNIER SCREW 01/19/2023
TORNIER INC PERFORM REV INSERT SZ 3/4, 39MM DIA, +0 01/19/2023
TORNIER INC TORNIER PERFORM REVERSED STAND ARD GLEN 01/19/2023
TORNIER INC UNKNOWN TORNIER SCREW 01/19/2023
-
-