• 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
 

 
 < 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 16 
 17 
 18 
 > 
 
404 records meeting your search criteria returned- Product Code: OCL Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC, INC. CRYOFLEX SURGICAL ABLATION PROBE 08/04/2022
ATRICURE, INC. ISOLATOR® SYNERGY¿ ENCOMPASS CLAMP AND G 07/15/2022
ATRICURE, INC. ISOLATOR SYNERGY ACCESS CLAMP 07/06/2022
ATRICURE, INC. "ISOLATOR SYNERGY"" ENCOMPASS CLAMP AND 06/16/2022
ATRICURE, INC. CANNULA ACCESSORIES 04/21/2022
PERFUSION SYSTEMS CARDIOBLATE 04/20/2022
MEDTRONIC, INC. CRYOFLEX SURGICAL ABLATION PROBE 04/20/2022
PERFUSION SYSTEMS CARDIOBLATE 04/04/2022
MEDTRONIC, INC. CRYOFLEX SURGICAL ABLATION PROBE 04/04/2022
ATRICURE, INC. ISOLATOR SYNERGY ENCOMPASS CLAMP AND GUI 03/03/2022
-
-