• 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
 

 
 
6 records meeting your search criteria returned- Product Code: OWY Patient Problem: Unspecified Infection Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITH & NEPHEW, INC. BIOINDUCTIVE IMPLANT W ARTHRO DEL LRG 12/18/2023
SMITH & NEPHEW, INC. BIOINDUCTIVE IMPLANT W/ARTH DEL MED 11/08/2023
SMITH & NEPHEW, INC. BIOINDUCTIVE IMPLANT W ARTHRO DEL MED 09/18/2023
SMITH & NEPHEW, INC. BIOINDUCTIVE IMPLANT W/ARTH DEL MED 12/22/2021
SMITH & NEPHEW, INC. BIOINDUCTIVE IMPLANT W/ARTH DEL LRG 05/13/2021
SMITH & NEPHEW, INC. TENDON ANCHORS 8 12/17/2020
-
-