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 
 > 
 
60 records meeting your search criteria returned- Product Code: MAX Patient Problem: Unspecified Tissue Injury Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SYNTHES GMBH UNK - CAGE/SPACERS: T-PAL 01/04/2024
SYNTHES GMBH UNK - CAGE/SPACERS: OPAL 01/04/2024
SYNTHES GMBH UNK - CAGE/SPACERS: T-PAL 01/04/2024
SYNTHES GMBH UNK - CAGE/SPACERS: T-PAL 01/03/2024
SYNTHES GMBH UNK - CAGE/SPACERS: OPAL 06/26/2023
MEDOS INTERNATIONAL SàRL CH UNK - CAGE/SPACER: CONDUIT EIT - TLIF 06/26/2023
MEDOS INTERNATIONAL SàRL CH UNK - CAGE/SPACER: CONDUIT 06/26/2023
MEDOS INTERNATIONAL SàRL CH UNK - CAGE/SPACER: CONDUIT 03/24/2023
MEDOS INTERNATIONAL SàRL CH UNK - CAGE/SPACER: CONDUIT 03/24/2023
SYNTHES GMBH UNK - CAGE/SPACERS: ACIS 02/15/2023
-
-