• 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 
 > 
 
73 records meeting your search criteria returned- Product Code: HTD Product Problem: Device-Device Incompatibility Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SYNTHES GMBH PERCUTANEOUS ARM 255MM 04/09/2024
SYNTHES GMBH COLLINEAR REDUCTION CLAMP SLIDING MECHAN 03/15/2024
SYNTHES GMBH STRAIGHT/CURVED POINTED REDUCTION FORCEP 02/05/2024
SYNTHES GMBH PELVIC ARM 225MM 01/09/2024
SYNTHES GMBH SLIDING MECHANISM 12/14/2023
SYNTHES GMBH RED FORCEPS POINTS NARROW-RATCHET 132 12/06/2023
SYNTHES GMBH SILIC HAND W/AO/ASIF-QC 12/01/2023
SYNTHES GMBH PERCUTANEOUS ARM 255MM 11/29/2023
SYNTHES GMBH COLLINEAR REDUCTION CLAMP SLIDING MECHAN 11/17/2023
SYNTHES GMBH HOHMANN-SHAPE ARM F/COLLIN REDUC CLAMP 11/17/2023
-
-