• 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 
 > 
 
81 records meeting your search criteria returned- Product Code: OTP Patient Problem: Unspecified Infection Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BOSTON SCIENTIFIC CORPORATION UPHOLD LITE 02/15/2023
ETHICON INC. ANTERIOR PELVIC FLOOR REPAIR S 01/17/2023
ETHICON INC. PROLIFT +M PELVIC FLOOR REPAIR UNKNOWN P 12/14/2022
BOSTON SCIENTIFIC CORPORATION PINNACLE 11/14/2022
BOSTON SCIENTIFIC CORPORATION UPHOLD VAGINAL SUPPORT SYSTEM 09/27/2022
ETHICON INC. PROLIFT PELVIC FLOOR REPAIR UNKNOWN PROD 04/28/2022
ETHICON INC. PROSIMA POSTERIOR SYSTEM 04/20/2022
ETHICON INC. TOTAL PELVIC FLOOR REPAIR SYST 04/20/2022
C.R. BARD, INC. (COVINGTON) -1018233 AVAULTA PLUS POSTERIOR BIOSYNTHETIC SUPP 04/20/2022
C.R. BARD, INC. (COVINGTON) -1018233 AVAULTA PLUS ANTERIOR BIOSYNTHETIC SUPPO 04/20/2022
-
-