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

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
 

 
 
7 records meeting your search criteria returned- Product Code: FAS Product Problem: Improper or Incorrect Procedure or Method Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
GREENWALD SURGICAL COMPANY, INC. GREENWALD SURGICAL CO., INC. 06/10/2021
GREENWALD SURGICAL COMPANY, INC. GREENWALD SURGICAL CO, INC. 05/12/2021
GREENWALD SURGICAL COMPANY, INC GREENWALD SURGICAL COMPANY, INC. 11/18/2020
GREENWALD SURGICAL COMPANY, INC. GREENWALD SURGICAL COMPANY, INC. 11/18/2020
GREENWALD SURGICAL COMPANY, INC. GREENWALD SURGICAL COMPANY, INC. 07/23/2020
RICHARD WOLF GMBH CUTTING ELECTRODE BIPO 24CH 12/30 09/18/2018
OLYMPUS WINTER & IBE GMBH HF-RESECTION ELECTRODE, LOOP, 24 FR., 0. 03/09/2015
-
-