• 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 
 3 
 4 
 > 
 
39 records meeting your search criteria returned- Product Code: FTL Product Problem: Unsealed Device Packaging Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DAVOL INC., SUB. C.R. BARD, INC. 3DMAX 04/25/2017
JOHNSON & JOHNSON INTERNATIONAL ULTRAPRO PLUG 04/10/2017
JOHNSON & JOHNSON INTERNATIONAL PROCEED VENTRAL PATCH 03/23/2017
DAVOL INC., SUB. C.R. BARD, INC. 3DMAX 02/07/2017
DAVOL INC., SUB. C.R. BARD, INC. PERFIX LIGHT PLUG 12/14/2016
DAVOL INC., SUB. C.R. BARD, INC. PERFIX LIGHT PLUG 12/12/2016
JOHNSON & JOHNSON INTERNATIONAL ULTRAPRO PLUG 12/01/2016
ETHICON INC. PROLENE POLYPROPYLENE MESH 11/09/2016
ETHICON INC. ULTRAPRO PLUG 06/07/2016
ETHICON INC. PHYSIOMESH OVAL 05/05/2016
-
-