• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

  • 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 
 
 
11 records meeting your search criteria returned- Product Code: PEW Patient Problem: Insufficient Information Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
HUDSON RESPIRATORY CARE TECATE S. DE R.L UROLIFT 08/29/2023
NEOTRACT, INC. UROLIFT SYSTEM 01/25/2023
NEOTRACT, INC. NEOTRACT UROLIFT SYSTEM 06/02/2022
NEOTRACT, INC. UROLIFT 03/29/2022
TELEFLEX INCORPORATED UROLIFT 03/09/2022
NEOTRACT, INC. UROLIFT IMPLANTS 05/18/2021
NEOTRACT, INC. UROLIFT 03/10/2021
NEOTRACT, INC. UROLIFT 09/17/2020
NEOTRACT, INC. UROLIFT 09/17/2020
NEOTRACT, INC. UROLIFT 09/17/2020
-
-