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

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 
 > 
 
12 records meeting your search criteria returned- Product Code: HIH Product Problem: Device Inoperable Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITH & NEPHEW, INC. SVCE REP HANDPIECE HYSTER MORCELLATOR 11/27/2017
SMITH & NEPHEW, INC. TRUCLEAR HANDPIECE 11/27/2017
SMITH & NEPHEW, INC. TRUCLEAR FOOTSWITCH 11/22/2017
HOLOGIC INC, MYOSURE XL HYSTEROSCOPIC TISSUE REMOVAL 11/09/2016
HOLOGIC INC MYOSURE 11/23/2015
SMITH & NEPHEW, INC. TRUCLEAR HANDPIECE 10/28/2015
HOLOGIC, INC. MYOSURE 09/25/2015
HOLOGIC MYOSURE TISSUE REMOVAL DEVICE 09/10/2015
SMITH & NEPHEW, INC. TRUCLEAR ULTRA RECIPROCATING MORC. 4.0 06/12/2015
SMITH & NEPHEW, INC. TRUCLEAR INCISOR PLUS BLADE 2.9 06/09/2015
-
-