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 
 > 
 
466 records meeting your search criteria returned- Product Code: MBI Product Problem: Migration or Expulsion of Device Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITH & NEPHEW, INC. BIORAPTOR CRV 2.3 PK SA UB COBRD BLUE 12/29/2021
SMITH & NEPHEW, INC. DYNOMITE 2.0 PK W/NDL 12-0 ULTRABRAID 12/27/2021
SMITH & NEPHEW, INC. TWINFIX TI 3.5 ULTRABRAID 11/01/2021
SMITH & NEPHEW, INC. HEALICOIL KNOTLESS PK ST 09/20/2021
SMITH & NEPHEW, INC. HEALICOIL KNOTLESS PK ST 09/20/2021
ZIMMER BIOMET, INC. JUGGERKNOT 1.4MM SHRT W/NDLS 04/12/2021
SMITH & NEPHEW, INC. SUTUREFIX ULTRA AHR S W/2 UB STR 1 BL 04/10/2021
ARTHROCARE CORP. MULTIFIX S-ULTRA 5.5MM KNOTLESS ANCHOR 12/11/2020
SMITH & NEPHEW, INC. FOOTPRINT ULTRA PK SUTURE ANCHOR 5.5 11/13/2020
MEDOS INTERNATIONAL SARL TRUESPAN 12 DEGREE PEEK 11/13/2020
-
-