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 
 > 
 
15 records meeting your search criteria returned- Product Code: MEH Patient Problem: Host-Tissue Reaction Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. M/L TAPER FEMORAL STEM 02/02/2021
ZIMMER BIOMET, INC. FEMORAL STEM 12/14 NECK TAPER PLASMA SPR 01/14/2021
ZIMMER BIOMET, INC. ECHO POR FEMORAL NC 15X155MM 09/16/2020
ZIMMER BIOMET, INC. FEMORAL STEM 12/14 NECK TAPER PLASMA SPR 07/31/2020
ZIMMER BIOMET, INC. FEMORAL STEM 12/14 NECK TAPER PLASMA SPR 12/16/2019
ZIMMER BIOMET, INC. ML TAPER SZ12.5 STD OFFSET 08/22/2018
BIOMET UK LTD. UNKNOWN M2A-MAGNUM 01/10/2017
DEPUY IRELAND ¿ 9616671 S-ROM*SLEEVE PRX ZT HA 16D-LRG 12/21/2015
STRYKER ORTHOPAEDICS CORK LRG TAP PRI MOD NCK 0DEG 38MM 04/22/2015
STRYKER ORTHOPAEDICS CORK UNK REJUVENATE/ABGII NECK 01/22/2015
-
-