• 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
 

 
 < 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 > 
 
360 records meeting your search criteria returned- Product Code: FTM Product Problem: Insufficient Information Report Date From: 01/1/2016
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
AROA BIOSURGERY OVITEX REINFORCED BIOSCAFFOLD 10/11/2019
DAVOL INC., SUB. C.R. BARD, INC. XENMATRIX 09/23/2019
AROA BIOSURGERY OVITEX REINFORCED BIOSCAFFOLD 08/09/2019
AROA BIOSURGERY LTD. OVITEX REINFORCED BIOSCAFFOLD 08/08/2019
DAVOL INC., SUB. C.R. BARD, INC. XENMATRIX 08/07/2019
DAVOL INC., SUB. C.R. BARD, INC. XENMATRIX 07/24/2019
DAVOL INC., SUB. C.R. BARD, INC. XENMATRIX 07/24/2019
DAVOL INC., SUB. C.R. BARD, INC. XENMATRIX 07/24/2019
ACELL, INC. GENTRIX SURGICAL MATRIX PLUS 06/12/2019
AROA BIOSURGERY OVITEX REINFORCED BIOSCAFFOLD 06/10/2019
-
-