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 
 > 
 
199 records meeting your search criteria returned- Product Code: MAI Product Problem: Device Dislodged or Dislocated Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ARTHREX, INC. DBL LOADED 4.75MM PEEK SWVLK 04/12/2024
ARTHREX, INC. SUTR ANCH PEEK S-TAK KNOTLESS 3X12.7MM 04/11/2024
ARTHREX, INC. 4.75MM PEEK KNOTLESS SWIVELOCK 04/11/2024
ARTHREX, INC. BIO-COMP SWVLK 3.5X 15.8MM 04/10/2024
ARTHREX, INC. DX KNOTLESS SWIVELOCK, BC, 4.75 MM 04/10/2024
ARTHREX, INC. PEEK SWIVELOCK C,4.75X19.1MM 04/09/2024
SMITH & NEPHEW, INC. MICRORAPTOR RGNSB SA UB II #1 STR BL CB 04/08/2024
ARTHREX, INC. SUTURE ANCHOR, BIO- COMPOSITE SUTURETAK 04/02/2024
ARTHREX, INC. SUTURE ANCHOR, BIO- COMPOSITE SUTURETAK 04/01/2024
SMITH & NEPHEW, INC. OSTEORAPTOR 2.9 W/ 2 UB WHITE / BLUE 03/27/2024
-
-