• 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
 

 
 
6 records meeting your search criteria returned- Product Code: KWP Product Problem: Patient Device Interaction Problem Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SYNTHES GMBH ROD ø3.5 PREBENT L240 TAN 01/12/2024
SYNTHES GMBH ROD ø3.5 PREBENT L240 TAN 01/12/2024
SYNTHES GMBH 4.0MM TI CORTEX EXPANSIONHEAD SCREW SELF 12/02/2021
WRIGHTS LANE SYNTHES USA PRODUCTS LLC TI MATRIX TOP LOADING POLYAXIAL HEAD 05/25/2021
MDT SOFAMOR DANEK PUERTO RICO MFG CD HORIZON SPINAL SYSTEM 11/24/2020
AESCULAP AG COLLECT.NO.QAS SPINE ANTERIOR STABILIS. 10/29/2020
-
-