• 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
 

 
 
10 records meeting your search criteria returned- Product Code: MBI Patient Problem: Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ARTHREX, INC. KNOTLESS HIP FIBERTAK 12/27/2022
ARTHREX, INC. KNOTLESS HIP FIBERTAK 12/27/2022
STRYKER ENDOSCOPY-SAN JOSE FG, CINCHLOCK SS ANCHOR WITH INSERTER 10/21/2022
ARTHREX, INC. NANO CORKSCREW FT, TI, W 3-0 FW 07/05/2022
STRYKER ENDOSCOPY-SAN JOSE ICONIX 1 NEEDLES WITH INTELLIBRAID TECHN 06/20/2022
ARTHREX, INC. FIBERTAK WITH SUTURETAPE 06/13/2022
ARTHREX, INC. FIBERTAK 02/21/2022
ARTHREX, INC. H/W INTERNALBRACE LGMNT AUGMNT REPR KIT 01/11/2022
ARTHREX, INC. KNOTLESS HIP FIBERTAK 12/07/2021
PARAGON 28, INC. TENOTAC SOFT TISSUE FIXATION SYSTEM 02/10/2021
-
-