• 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 
 > 
 
199 records meeting your search criteria returned- Product Code: HSD Patient Problem: Joint Laxity Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ENCORE MEDICAL L.P ALTIVATE ANATOMIC, SHORT HUMERAL STEM, 1 12/06/2023
DEPUY INTERNATIONAL LTD - 8010379 DXTEND STAND PE CUP D38 +6MM 11/30/2023
DEPUY IRELAND - 9616671 DXTEND STAND PE CUP D42 +6MM 11/21/2023
ENCORE MEDICAL L.P. ALTIVATE REVERSE, HUMERAL STEM, STANDARD 11/07/2023
DEPUY IRELAND - 9616671 DXTEND STAND PE CUP D42 +6MM 11/06/2023
DEPUY IRELAND - 9616671 UNKNOWN SHOULDER METAGLENE 11/01/2023
DEPUY ORTHOPAEDICS INC US DXTEND STAND PE CUP D38 +6MM 10/31/2023
ZIMMER BIOMET, INC. MD HYBRID GLENOID BASE 4MM 10/05/2023
ZIMMER BIOMET, INC. VERSA-DIAL 46X18X53 HUM HEAD 10/05/2023
DEPUY INTERNATIONAL LTD - 8010379 DXTEND STAND PE CUP D38 +9MM 09/28/2023
-
-