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 
 > 
 
24 records meeting your search criteria returned- Product Code: OCW Product Problem: Difficult to Remove Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
APOLLO ENDOSURGERY OVERSTITCH ENDOSCOPIC SUTURING SYSTEM 12/21/2020
APOLLO ENDOSURGERY OVERSTITCH ENDOSCOPIC SUTURING SYSTEM 11/23/2020
APOLLO ENDOSURGERY OVERSTITCH ENDOSCOPIC SUTURING SYSTEM 11/19/2020
COVIDIEN ENDOSTITCH SUTURING DEVICE 10/08/2020
COVIDIEN 0 POLYSORB ENDOSTITCH 10/08/2020
COVIDIEN 0 POLYSORB ENDOSTITCH 10/08/2020
COVIDIEN 0 POLYSORB ENDOSTITCH 10/08/2020
COVIDIEN LP ENDO STITCH 06/29/2020
APOLLO ENDOSURGERY, INC. OVERSTITCH¿ ENDOSCOPIC SUTURING SYSTEM 01/20/2020
APOLLO ENDOSURGERY, INC. OVERSTITCH¿ ENDOSCOPIC SUTURING SYSTEM 01/07/2020
-
-