• 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 
 > 
 
24 records meeting your search criteria returned- Product Code: JWH Product Problem: Peeled/Delaminated Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER MANUFACTURING B.V. NEXGEN ALL POLY PETELLA STANDARD CEMENTE 04/25/2024
EXACTECH, INC. OPTETRAK LOGIC 03/06/2024
EXACTECH, INC. OPTETRAK 02/27/2024
ZIMMER BIOMET, INC. VNGD CR TIB BRG 12/21/2023
ZIMMER BIOMET, INC. ALL POLY PETELLA STANDARD CEMENTED SIZE 12/20/2023
ZIMMER BIOMET, INC. UNKNOWN PATELLA 12/19/2023
SMITH & NEPHEW, INC. GII PS HI FLEX ISRT SZ 3-4 9 06/12/2023
EXACTECH, INC. OPTETRAK KNEE 07/14/2022
SMITH & NEPHEW, INC. UNKN GENESIS KNEE INSTR 02/10/2022
DEPUY ORTHOPAEDICS INC US UNK FEMORAL TRIAL 02/09/2022
-
-