Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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 
 > 
 
47 records meeting your search criteria returned- Product Code: JDH Patient Problem: No Known Impact Or Consequence To Patient Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITH & NEPHEW ORTHOPAEDICS AG POLARCUP INTRODUCER ROTATION PLATE 06/10/2020
SMITH & NEPHEW ORTHOPAEDICS AG FEM HEAD AARAU 06/10/2020
SMITH & NEPHEW, INC. R3 LINER CERAMIC POLY 06/02/2020
SMITH & NEPHEW, INC. UNKNOWN REDAPT STEM 05/20/2020
SMITH & NEPHEW, INC. UNKNOWN ORTHOPAEDIC RECONSTRUCTION DEV 05/19/2020
SMITH & NEPHEW, INC. UNKN ORTHOPAEDIC RECONSTRUCTION DEV 05/15/2020
SMITH & NEPHEW ORTHOPAEDICS AG UNKN. POLARSTEM (UNKN. TYPE) 03/17/2020
SMITH & NEPHEW, INC. UNKNOWN 03/01/2020
SMITH & NEPHEW, INC. TNDM BP SHL/XLPE LNR 51OD 26ID 02/14/2020
SMITH & NEPHEW, INC. HIP IMPLANT 02/04/2020
-
-