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 
 > 
 
102 records meeting your search criteria returned- Product Code: MBI Product Problem: Device Slipped Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
PARAGON 28, INC. TENOTAC SOFT TISSUE FIXATION SYSTEM 12/09/2020
STRYKER CORPORATION OMEGA 11/18/2020
ARTHREX, INC. FIBERTAK 11/16/2020
STRYKER ENDOSCOPY-SAN JOSE OMEGA 4.75MM PEEK KNOTLESS ANCHOR SYSTEM 10/13/2020
ARTHREX, INC. DX FIBERTAK SUTURE ANCHOR, ST & NDLS 04/22/2020
ARTHROCARE CORP. 2.8MM Q-FIX ALL SUTURE ANCHOR 02/11/2020
ARTHREX, INC. FIBERTAK BICEPS IMPLANT SET 01/20/2020
ARTHREX, INC. FIBERSTITCH IMPLANT, CURVED 12/26/2019
SMITH & NEPHEW, INC. TWINFIX ULTRA PK 4.5MM W/2 UB -WHT &BL 08/31/2019
ARTHROCARE CORP. MAGNUM 2 KNOTLESS IMPLANT 04/16/2019
-
-