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

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 
 7 
 > 
 
65 records meeting your search criteria returned- Product Code: FDF Product Problem: Fracture Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
AIZU OLYMPUS CO., LTD. EVIS EXERA III COLONOVIDEOSCOPE 08/31/2023
AIZU OLYMPUS CO., LTD. EVIS EXERA III COLONOVIDEOSCOPE 08/31/2023
SHIRAKAWA OLYMPUS CO., LTD. MAINTENANCE UNIT 02/03/2023
HOYA CORPORATION PENTAX TOKYO OFFICE PENTAX 05/20/2022
HOYA CORPORATION PENTAX TOKYO OFFICE PENTAX 05/20/2022
OLYMPUS MEDICAL SYSTEMS CORP. MAINTENANCE UNIT 04/14/2022
HOYA CORPORATION PENTAX TOKYO OFFICE PENTAX 02/28/2022
HOYA CORPORATION PENTAX TOKYO OFFICE PENTAX 02/28/2022
HOYA CORPORATION PENTAX TOKYO OFFICE PENTAX 02/17/2022
HOYA CORPORATION PENTAX TOKYO OFFICE PENTAX 01/06/2022
-
-