• 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 
 3 
 4 
 5 
 6 
 > 
 
54 records meeting your search criteria returned- Product Code: MBI Product Problem: Loose or Intermittent Connection Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ARTHREX, INC. TIGHTROPE ® II RT WITH DEPLOYING SUTURE 12/12/2022
ARTHREX, INC. FIBERTAK 07/05/2022
ARTHREX, INC. FIBERTAK 10/12/2021
ARTHREX, INC. FIBERTAK 08/17/2021
PARAGON 28, INC. TENOTAC SOFT TISSUE FIXATION SYSTEM 02/04/2021
ARTHREX, INC. DX FIBERTAK SUTURE ANCHOR, ST & NDLS 01/05/2021
ARTHROCARE CORP. QFIX 1.8 MINI SUTURE ANCHOR 12/18/2020
PARAGON 28, INC. TENOTAC SOFT TISSUE FIXATION SYSTEM 11/25/2020
MEDOS INTERNATIONAL SARL TRUESPAN 12 DEGREE PEEK 11/17/2020
MEDOS INTERNATIONAL SàRL CORTICAL FXATION FXD LOOP 40MM 10/21/2020
-
-