• 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
 

 
 
4 records meeting your search criteria returned- Product Code: PNZ Report Date From: 1/1/2017 Report Date To: 12/31/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ACCLARENT, INC. ACCLARENT AERA 10/10/2017
ENTELLUS MEDICAL XPRESS LOPROFILE ENT DILATION SYSTEM 07/24/2017
ENTELLUS MEDICAL SINUS BALLOON 07/01/2017
ACCLARENT, INC. AERA EUSTACHIAN TUBE BALLOON DILATION SY 01/18/2017
-
-