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
 

 
 
10 records meeting your search criteria returned- Product Code: EOQ Product Problem: Deformation Due to Compressive Stress Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
INTUITIVE SURGICAL, INC ION 12/22/2023
AIZU OLYMPUS CO., LTD. BRONCHOFIBERSCOPE 11/21/2023
AIZU OLYMPUS CO., LTD. BRONCHOFIBERSCOPE 11/13/2023
AIZU OLYMPUS CO., LTD. EVIS LUCERA ELITE BRONCHOVIDEOSCOPE 08/31/2023
AIZU OLYMPUS CO., LTD. BRONCHOVIDEOSCOPE 05/02/2023
AIZU OLYMPUS CO., LTD. BRONCHOFIBERSCOPE 08/05/2022
OLYMPUS MEDICAL SYSTEMS CORP. BRONCHOFIBERSCOPE 03/07/2022
VERATHON MEDICAL ULC GLIDESCOPE BFLEX 5.0 SINGLE-USE BRONCHOS 01/11/2022
HOYA CORPORATION PENTAX TOKYO OFFICE PENTAX 01/06/2022
HOYA CORPORATION PENTAX TOKYO OFFICE PENTAX 07/20/2021
-
-