• 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 
 > 
 
14 records meeting your search criteria returned- Product Code: JDR Patient Problem: Post Operative Wound Infection Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITH & NEPHEW, INC. MNITAC 2.0 TI W/NDL 22-0 ULTRABRAID 12/06/2022
SMITH & NEPHEW, INC. TWINFIX TI 3.5 ULTRABRAID 11/17/2022
SMITH & NEPHEW, INC. UNKN METAL SUTURE ANCHOR 11/30/2021
WRIGHTS LANE SYNTHES USA PRODUCTS LLC UNK - BME 08/24/2021
WRIGHTS LANE SYNTHES USA PRODUCTS LLC UNK - BONE STAPLE: ELITE 08/24/2021
WRIGHTS LANE SYNTHES USA PRODUCTS LLC UNK - BONE STAPLE 03/18/2021
WRIGHTS LANE SYNTHES USA PRODUCTS LLC UNK - BONE STAPLE: ELITE 02/01/2021
WRIGHTS LANE SYNTHES USA PRODUCTS LLC UNK - BONE STAPLE: ELITE 02/01/2021
STRYKER GMBH UNKNOWN STIRRUP WIRE 06/23/2020
STRYKER GMBH UNKNOWN EASYCLIP STAPLE 06/08/2020
-
-