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

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
 

 
 
8 records meeting your search criteria returned- Product Code: MBI Product Problem: Fitting Problem Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ARTHREX, INC. KL 1.8 FIBERTAK, SHOULDER 02/28/2024
ARTHREX, INC. FIBERLOCK SUSPENSION SYSTEM 01/23/2024
ARTHREX, INC. TIGHTROPE ® II RT WITH DEPLOYING SUTURE 01/22/2024
ARTHREX, INC. FIBERTAK 01/10/2024
ARTHREX, INC. TIGHTROPE ® II BTB WITH DEPLOYING SUTURE 12/07/2023
ARTHREX, INC. DOUBLE LOADED KNOTLESS FIBERTAK, KNEE 09/14/2023
ARTHREX, INC. 2.6 MM KNOTLESS FIBERTAK ANCHOR 07/05/2022
SMITH & NEPHEW, INC. TWINFIX ULTRA 4.5MM W/2 UB (BLK &BLUE) 10/20/2021
-
-