• 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 
 
 
19 records meeting your search criteria returned- Product Code: OCW Patient Problem: Pain Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
APOLLO ENDOSURGERY, INC. OVERSTITCH¿ ENDOSCOPIC SUTURING SYSTEM 06/21/2022
APOLLO ENDOSURGERY OVERSTITCH ENDOSCOPIC SUTURING SYSTEM 04/28/2021
APOLLO ENDOSURGERY OVERSTITCH ENDOSCOPIC SUTURING SYSTEM 04/01/2021
DAVIS & GECK CARIBE LTD UNKNOWN VLOC ENDO STITCH RELOAD ABS 11/05/2019
APOLLO ENDOSURGERY, INC. OVERSTITCH ENDOSCOPIC SUTURING SYSTEM 06/14/2019
APOLLO ENDOSURGERY, INC. OVERSTITCH ENDOSCOPIC SUTURING SYSTEM 06/07/2019
APOLLO ENDOSURGERY, INC. OVERSTITCH ENDOSCOPIC SUTURING SYSTEM 06/05/2019
COVIDIEN PROTAK 03/19/2019
DAVIS & GECK CARIBE LTD ENDO STITCH 02/24/2019
-
-