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 
 6 
 
 
51 records meeting your search criteria returned- Product Code: OPR Product Problem: Device Dislodged or Dislocated Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MICROVENTION, INC. WEB SL 12/21/2021
MICROVENTION, INC. WEB SLS 06/18/2021
MICROVENTION, INC. WEB SL 21 SINGLE LAYER 06/09/2021
MICROVENTION, INC. WEB SL 05/28/2021
MICROVENTION, INC. WEB SLS 04/20/2021
MICROVENTION, INC. WEB SL 04/08/2021
MICROVENTION, INC. WEB SL 03/24/2021
SEQUENT MEDICAL, INC. WEB LOW PROFILE SL-USA W4-5-3FOR US 07/09/2020
SEQUENT MEDICAL, INC WEB SL 17 SINGLE LAYER W5-7-4 11/01/2019
SEQUENT MEDICAL, INC WEB ANEURYSM EMBOLIZATION DEVICE 10/27/2019
-
-