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: MAX Product Problem: Improper or Incorrect Procedure or Method Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
INNOVASIS, INC. TX IBF SYSTEM 08/15/2024
GLOBUS MEDICAL, INC. SABLE 03/05/2024
GLOBUS MEDICAL, INC. SABLE 03/05/2024
SPINEOLOGY INC. ELITE EXPANDABLE INTERBODY FUSION DEVICE 08/25/2023
STRYKER SPINE-US 9MM X 6DEG X 9MM X 23MM 06/09/2023
LDR MÉDICAL ROI-A INSET MEDIAN IMPLANT H16MM 30X39MM 01/27/2023
NEUROPRO SPINAL JAXX NEUROPRO SPINAL JAXX 12/08/2022
INNOVASIS, INC. TXTIHA IBF SYSTEM 11/29/2022
STRYKER SPINE-US 10X23X12DEG-11 11/04/2022
CORELINK SURGICAL, LLC EXPANDABLE INTERBODIES 11/12/2021
-
-