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 
 6 
 7 
 8 
 9 
 10 
 > 
 
195 records meeting your search criteria returned- Product Code: MBH Product Problem: Detachment of Device or Device Component Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. ARTICULAR SURFACE ULTRACONGRUENT SIZE 00 06/20/2023
STRYKER ORTHOPAEDICS-MAHWAH TRIATHLON MB PATELLA PA A38 06/19/2023
ZIMMER BIOMET, INC. NONPOROUS STEMMED TIBIAL BASEPLATE SIZE 05/16/2023
ZIMMER BIOMET, INC. TIBIAL ARTICULAR SURFACE PROVISIONAL SHI 05/03/2023
STRYKER ORTHOPAEDICS-MAHWAH TRIATHLON CR X3 TIBIAL INSERT 04/26/2023
STRYKER ORTHOPAEDICS-MAHWAH TRIATHLON MB PATELLA PA A35 04/24/2023
STRYKER ORTHOPAEDICS-MAHWAH TRIATHLON CR FEM COMP #5 L-CEM 03/31/2023
ZIMMER BIOMET, INC. TIBIAL ARTICULAR SURFACE PROVISIONAL SHI 03/28/2023
ZIMMER BIOMET, INC. TIBIAL ARTICULAR SURFACE PROVISIONAL SHI 03/14/2023
ZIMMER BIOMET, INC. TIBIAL ARTICULAR SURFACE PROVISIONAL SHI 03/02/2023
-
-