• 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 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
111 records meeting your search criteria returned- Product Code: HWT Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY IRELAND 9616671 ATTUNE PS FEM TRIAL SZ 5 RT 11/30/2021
DEPUY IRELAND - 9616671 ATTUNE PS FEM TRIAL SZ 9 RT 11/29/2021
DEPUY IRELAND - 9616671 ATTUNE PS FEM TRIAL SZ 6 RT 11/07/2021
DEPUY ORTHOPAEDICS INC US UNK FEMORAL TRIAL 10/06/2021
MICROPORT ORTHOPEDICS INC. ACETABULAR CUP 09/09/2021
DEPUY IRELAND - 9616671 RECLAIM PROX NECK TRL 40MM 08/25/2021
DEPUY IRELAND - 9616671 ATTUNE SPACER BLOCK 08/03/2021
ZIMMER BIOMET, INC. BIOMET LO PRO SPH MILL MED 07/30/2021
DEPUY IRELAND - 9616671 ATTUNE RP PS ARTIC SURF SZ6 07/27/2021
DEPUY IRELAND - 9616671 ATTUNE PS FEM TRIAL SZ 8 LT 07/14/2021
-
-