• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

  • 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 
 > 
 
55 records meeting your search criteria returned- Product Code: JEY Patient Problem: Unspecified Tissue Injury Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SYNTHES GMBH UNK - RAPIDSORB IPS IMPLANTS 02/21/2024
A&E MEDICAL CORPORATION MYO/WIRE UFM W 89MM KN 01/05/2024
SYNTHES GMBH TI LOW PROFILE NEURO SCREW SELF-DRILLING 12/12/2023
SYNTHES GMBH TI LOW PROFILE NEURO SCREW SELF-DRILLING 12/12/2023
SYNTHES GMBH TI LOW PROFILE NEURO SCREW SELF-DRILLING 12/12/2023
SYNTHES GMBH TI LOW PROFILE NEURO SCREW SELF-DRILLING 12/12/2023
SYNTHES GMBH TI LOW PROFILE NEURO SCREW SELF-DRILLING 12/12/2023
SYNTHES GMBH TI LOW PROFILE NEURO SCREW SELF-DRILLING 12/12/2023
SYNTHES GMBH TI LOW PROFILE NEURO SCREW SELF-DRILLING 12/12/2023
SYNTHES GMBH TI LOW PROFILE NEURO SCREW SELF-DRILLING 12/12/2023
-
-