• 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 
 > 
 
63 records meeting your search criteria returned- Product Code: OOD Patient Problem: Impaired Healing Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DAVOL INC., SUB. C.R. BARD, INC. -121364 PHASIX MESH 11/28/2023
DAVOL INC., SUB. C.R. BARD, INC. -121364 PHASIX MESH 10/22/2023
DAVOL INC., SUB. C.R. BARD, INC. -121364 PHASIX MESH 03/23/2023
TEPHA, INC. - 3005670760 GALAFLEX 02/13/2023
TEPHA, INC. - 3005670760 GALAFLEX 3DR 11/04/2022
TEPHA, INC. - 3005670760 GALAFLEX 11/02/2022
TEPHA, INC. - 3005670760 GALAFLEX 3D 11/02/2022
TEPHA, INC. - 3005670760 GALAFLEX 3DR 11/01/2022
TEPHA, INC. - 3005670760 GALAFLEX 08/02/2022
TEPHA, INC. - 3005670760 GALAFLEX 3DR 08/02/2022
-
-