• 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
 

 
 < 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 16 
 > 
 
163 records meeting your search criteria returned- Product Code: OWB Product Problem: Unintended Movement Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
PHILIPS HEALTHCARE ALLURA XPER FD20 07/21/2020
SIEMENS HEALTHCARE GMBH AXIOM LUMINOS DRF 06/23/2020
MEDTRONIC NAVIGATION, INC (LITTLETON) O2 06/03/2020
PHILIPS HEALTHCARE ALLURA XPER FD20 05/26/2020
MEDTRONIC NAVIGATION, INC (LITTLETON) O-ARM SYS BI70002000 O2 CD 120V B EN EN 12/13/2019
MEDTRONIC NAVIGATION, INC (LITTLETON) OARM O2 IMAGING SYSTEM 11/18/2019
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. ALLURA XPER FD10 09/05/2019
PHILIPS HEALTHCARE ALLURA XPER FD20 08/09/2019
MEDTRONIC NAVIGATION, INC (LITTLETON) O2 O-ARM IMAGING SYSTEM 07/23/2019
MEDTRONIC NAVIGATION, INC (LITTLETON) O-ARM O2 IMAGING SYSTEM 07/10/2019
-
-