• 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
 

 
 < 
 2 
 3 
 4 
 5 
 6 
 7 
 
 
69 records meeting your search criteria returned- Product Code: GFD Patient Problem: Insufficient Information Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER SURGICAL, INC. HANDPIECE, ELECTRIC DERMATOME 06/29/2021
ZIMMER SURGICAL, INC. ZIMMER AIR DERMATOME 06/14/2021
ZIMMER SURGICAL, INC. ZIMMER AIR DERMATOME 06/10/2021
ZIMMER SURGICAL, INC. ZIMMER AIR DERMATOME 06/08/2021
ZIMMER SURGICAL, INC. ZMR AIR DERMATOME HANDPIECE 05/17/2021
ZIMMER SURGICAL, INC. HANDPIECE, ELECTRIC DERMATOME 04/30/2021
ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, IN ZIMMER DERMATOME 04/12/2021
ZIMMER SURGICAL, INC. ZIMMER AIR DERMATOME 02/25/2021
ZIMMER SURGICAL, INC. HANDPIECE, ELECTRIC DERMATOME 01/11/2021
-
-