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 
 > 
 
49 records meeting your search criteria returned- Product Code: MRA Patient Problem: Inadequate Osseointegration Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITH & NEPHEW, INC. SPEC EF PRI SO 12/14 SZ 1 11/02/2022
ZIMMER MANUFACTURING B.V. BONE SCR 6.5X20 SELF-TAP 04/11/2022
SMITH & NEPHEW, INC. SPEC EF PRIM HO 12/14 SZ 4 03/17/2022
ZIMMER BIOMET, INC. BONE SCR 6.5X20 SELF-TAP 06/29/2021
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 01/04/2021
DEPUY ORTHOPAEDICS, INC. 1818910 SROM*STMLG36+21CR4L 16X11X205N 08/17/2020
DEPUY ORTHOPAEDICS, INC. 1818910 SROM STM STD 36+12L 13X18 07/21/2020
DEPUY ORTHOPAEDICS INC US PINNACLE SECTOR II CUP 50MM 07/10/2020
DEPUY ORTHOPAEDICS INC US SROM STM STD 36+12L 13X18 06/23/2020
DEPUY ORTHOPAEDICS INC US PINNACLE SECTOR II CUP 54MM 05/29/2020
-
-