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 
 > 
 
44 records meeting your search criteria returned- Product Code: OCW Patient Problem: Unspecified Tissue Injury Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DAVIS & GECK CARIBE LTD SURGIDAC 04/19/2022
DAVIS & GECK CARIBE LTD ENDO STITCH 12/27/2021
DAVIS & GECK CARIBE LTD ENDO STITCH 12/22/2021
DAVIS & GECK CARIBE LTD ENDO STITCH 12/06/2021
DAVIS & GECK CARIBE LTD POLYSORB 10/09/2021
DAVIS & GECK CARIBE LTD ENDO STITCH 10/09/2021
DAVIS & GECK CARIBE LTD ENDO STITCH 10/02/2021
DAVIS & GECK CARIBE LTD ENDO STITCH 06/17/2021
DAVIS & GECK CARIBE LTD ENDO STITCH 11/02/2020
DAVIS & GECK CARIBE LTD ENDO STITCH 11/02/2020
-
-