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
 

 
 < 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 > 
 
500 records meeting your search criteria returned. The results are incomplete - please narrow your search.

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITH & NEPHEW, INC. TWINFIX ULTRA 5.5MM W/2 UB (WHT & BLUE) 03/22/2024
ARTHREX, INC. KL 1.8 FIBERTAK, SHOULDER 03/22/2024
ARTHREX, INC. 2.6 MM KNOTLESS FIBERTAK ANCHOR 03/22/2024
SMITH & NEPHEW, INC. HEALICOIL KNOTLESS PK NST 03/22/2024
ARTHREX, INC. IMPLANT SYSTEM, FIBERTAK BUTTON 03/22/2024
ARTHREX, INC. TIGHTROPE ® II RT WITH DEPLOYING SUTURE 03/21/2024
ARTHREX, INC. KL 1.8 FIBERTAK, SHOULDER 03/21/2024
ARTHREX, INC. KL 1.8 FIBERTAK, SHOULDER 03/21/2024
SMITH & NEPHEW, INC. FOOTPRINT ULTRA PK SUTURE ANCHOR 4.5 03/21/2024
SMITH & NEPHEW, INC. HEALICOIL KNOTLESS PK NST 03/21/2024
-
-