• 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
 

 
 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
132 records meeting your search criteria returned- Product Code: MBI Patient Problem: Rupture Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITH & NEPHEW, INC. BONE ANCHORS 3 W ARTHRO DEL SYS ADVNCD 12/20/2023
SMITH & NEPHEW, INC. UNKNOWN PEEK SUTURE ANCHOR 09/17/2023
SMITH & NEPHEW, INC. BIORAPTOR KNOTLESS SUTURE ANCHOR 08/17/2023
SMITH & NEPHEW, INC. SUTUREFIX ULTRA AHR S 2 UB STR CB BLU 07/25/2023
SMITH & NEPHEW, INC. UNKNOWN SUSPENSORY FIXATION DEV 07/25/2023
SMITH & NEPHEW, INC. UNKN JOINT REPAIR DEV 07/21/2023
SMITH & NEPHEW, INC. SUTUREFIX ULTRA AHR S W/2 UB STR 1 BL 07/17/2023
SMITH & NEPHEW, INC. BIRPTR 2.3 PK SUTURE ANCHOR W/ ULTRAB 07/14/2023
SMITH & NEPHEW, INC. TWINFIX ULTRA PK 4.5MM W/2 UB -WHT &BL 06/27/2023
SMITH & NEPHEW, INC. FOOTPRINT ULTRA PK SUTURE ANCHOR 4.5 06/23/2023
-
-