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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
435 records meeting your search criteria returned- Product Code: MBI 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
MEDOS INTERNATIONAL SARL TRUESPAN 24 DEGREE PLGA 12/26/2023
MEDOS INTERNATIONAL SARL TRUESPAN 24 DEGREE PLGA 12/26/2023
ARTHREX, INC. TIGHTROPE® II BTB, RECON IB¿ 12/21/2023
SMITH & NEPHEW, INC. MICRORAPTOR KNOTLESS SA PEEK 12/18/2023
MEDOS INTERNATIONAL SàRL TRUESPAN 24 DEGREE PEEK 12/07/2023
MEDOS INTERNATIONAL SàRL TRUESPAN 24 DEGREE PEEK 12/07/2023
MEDOS INTERNATIONAL SàRL TRUESPAN 24 DEGREE PEEK 12/06/2023
MEDOS INTERNATIONAL SARL TRUESPAN 12 DEGREE PEEK 12/06/2023
ARTHREX, INC. FIBERTAG TIGHTROPE II ABS 12/05/2023
SMITH & NEPHEW, INC. SUTUREFIX ULTRA AHR S 2 UB STR BLUE 11/29/2023
-
-