• 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 
 > 
 
15 records meeting your search criteria returned- Product Code: FDS Product Problem: Deformation Due to Compressive Stress Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
HOYA CORPORATION PENTAX TOKYO OFFICE PENTAX 12/25/2023
AIZU OLYMPUS CO., LTD. GASTROINTESTINAL VIDEOSCOPE 12/07/2023
HOYA CORPORATION PENTAX TOKYO OFFICE PENTAX 09/20/2023
HOYA CORPORATION PENTAX TOKYO OFFICE PENTAX 09/08/2023
HOYA CORPORATION PENTAX TOKYO OFFICE PENTAX 04/27/2023
HOYA CORPORATION PENTAX TOKYO OFFICE PENTAX 04/25/2023
AIZU OLYMPUS CO., LTD. EVIS EXERA III GASTROINTESTINAL VIDEOSCO 12/06/2022
HOYA CORPORATION PENTAX TOKYO OFFICE PENTAX 03/08/2022
HOYA CORPORATION PENTAX TOKYO OFFICE PENTAX 02/12/2022
HOYA CORPORATION PENTAX TOKYO OFFICE PENTAX 11/15/2021
-
-