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

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
 

 
 
6 records meeting your search criteria returned- Product Code: LRC Product Problem: Unsealed Device Packaging Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ACCLARENT, INC. RELIEVA SPINPLUS NAV BALLOON SINUPLASTY 11/10/2021
ACCLARENT, INC. RELIEVA SPIN SINUPLASTY GUIDE 05/12/2016
ACCLARENT, INC. RELIEVA SPIN SINUPLASTY SYSTEM 11/10/2015
GYRUS ACMI, INC. DISPOSABLE MYR BLADE WITH HANDLE 10/14/2015
GYRUS ACMI, INC. DISPOSABLE MYR BLADE WITH HANDLE 10/14/2015
GYRUS ACMI, INC. DISPOSABLE MYR BLADE WITH HANDLE 10/14/2015
-
-