Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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 
 4 
 5 
 > 
 
42 records meeting your search criteria returned- Product Code: LRC Patient Problem: No Clinical Signs, Symptoms or Conditions Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ACCLARENT, INC. RELIEVA SPINPLUS NAV BALLOON SINUPLASTY 11/10/2021
COOK INC COOK DOUBLE LUMEN EXTRA FIRM SOFT TIPPED 09/10/2021
ACCLARENT, INC. RELIEVA SPINPLUS NAV BALLOON SINUPLASTY 08/04/2021
ACCLARENT, INC. RELIEVA SPINPLUS NAV BALLOON SINUPLASTY 08/04/2021
INTEGRA MICROFRANCE S.A.S. PRESS MCO820 FOR EAR IMPLANT MARTIN 06/30/2021
GYRUS ACMI, INC PORP TRIAL 2.0 MM 05/14/2021
ACCLARENT, INC. RELIEVA SPINPLUS NAV BALLOON SINUPLASTY 03/23/2021
COOK INC FROVA INTUBATING INTRODUCER 03/04/2021
COOK INC FROVA INTUBATING INTRODUCER 03/04/2021
ACCLARENT, INC. RELIEVA SPIN PLUS KIT, 3 GUIDES, 6MM, 5P 02/12/2021
-
-