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
 

 
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
300 records meeting your search criteria returned- Product Code: FZP Patient Problem: No Known Impact Or Consequence To Patient Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ETHICON ENDO-SURGERY, INC. LIGAMAX 5 04/29/2020
COVIDIEN ENDO CLIP III 04/15/2020
COVIDIEN ENDO CLIP III 04/15/2020
COVIDIEN ENDO CLIP III 04/13/2020
COVIDIEN ENDO CLIP III 04/13/2020
DAVIS & GECK CARIBE LTD ENDO CLIP 04/03/2020
ATRICURE, INC. ATRICLIP LAA EXCLUSION SYSTEM WITH PRELO 03/17/2020
ETHICON ENDO-SURGERY, INC. LIGAMAX 03/10/2020
MEDTRONIC / COVIDIEN COVIDIEN SURGICLIP M 11.5 03/09/2020
COVIDIEN COVIDIEN ENDO CLIP III 5MM 03/05/2020
-
-