• 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 
 7 
 8 
 9 
 10 
 > 
 
94 records meeting your search criteria returned- Product Code: GZB 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
NALU MEDICAL INC NALU NEUROSTIMULATION SYSTEM 10/26/2023
NEUROMED INC. NEUROSTIMULATION SYSTEM 08/12/2023
ABBOTT MEDICAL SWIFT-LOCK ANCHOR 08/02/2023
ABBOTT MEDICAL SWIFT-LOCK ANCHOR 07/11/2023
ABBOTT MEDICAL SWIFT-LOCK ANCHOR 06/05/2023
BOSTON SCIENTIFIC CORPORATION STIM KIT VERCISE 05/09/2023
NALU MEDICAL INC NALU NEUROSTIMULATION SYSTEM 05/01/2023
STIMWAVE TECHNOLOGIES INC. FREEDOM SPINAL CORD STIMULATOR 04/10/2023
MPRI N/A 03/27/2023
ABBOTT MEDICAL SWIFT-LOCK ANCHOR 02/28/2023
-
-