Stent, iliac vein

FDA product code QAN · Class 3 · 144 devices · 719 reports · 3 deaths reported · 90 devices named in recalls

• Abre™ AB9U16100090

  Medtronic, Inc. · Stent, iliac vein
  7 reports
• Abre™ AB9U16120090

  Medtronic, Inc. · Stent, iliac vein
  7 reports
• VICI VENOUS STENT ® SYSTEM H74916060100

  Veniti Inc · Stent, iliac vein
  7 reports
• Zilver Vena G57455

  Cook Ireland Ltd · Stent, iliac vein
  7 reports
• Zilver Vena G57451

  Cook Ireland Ltd · Stent, iliac vein
  6 reports
• Zilver Vena G57454

  Cook Ireland Ltd · Stent, iliac vein
  6 reports
• Abre™ AB9U12100090

  Medtronic, Inc. · Stent, iliac vein
  5 reports
• Abre™ AB9U16060090

  Medtronic, Inc. · Stent, iliac vein
  5 reports
• Abre™ AB9U18060090

  Medtronic, Inc. · Stent, iliac vein
  1 death5 reports
• Abre™ AB9U18120090

  Medtronic, Inc. · Stent, iliac vein
  5 reports
• VENOUS WALLSTENT™ H74912044208070

  Boston Scientific Corporation · Stent, iliac vein
  5 reports
• Abre™ AB9U12120090

  Medtronic, Inc. · Stent, iliac vein
  4 reports
• Abre™ AB9U20080090

  Medtronic, Inc. · Stent, iliac vein
  1 death4 reports
• VICI VENOUS STENT ® SYSTEM H74914060100

  Veniti Inc · Stent, iliac vein
  4 reports
• VENOUS WALLSTENT™ H74912044166070

  Boston Scientific Corporation · Stent, iliac vein
  4 reports
• VENOUS WALLSTENT™ H74912044186070

  Boston Scientific Corporation · Stent, iliac vein
  4 reports
• Zilver Vena G57453

  Cook Ireland Ltd · Stent, iliac vein
  4 reports
• Abre™ AB9U18080090

  Medtronic, Inc. · Stent, iliac vein
  3 reports
• VICI VENOUS STENT ® SYSTEM H74914090100

  Veniti Inc · Stent, iliac vein
  3 reports
• VICI VENOUS STENT ® SYSTEM H74914120100

  Veniti Inc · Stent, iliac vein
  3 reports
• VICI VENOUS STENT ® SYSTEM H74916090100

  Veniti Inc · Stent, iliac vein
  3 reports
• Zilver Vena G57434

  Cook Ireland Ltd · Stent, iliac vein
  3 reports
• Zilver Vena G57446

  Cook Ireland Ltd · Stent, iliac vein
  3 reports
• Abre™ AB9U18150090

  Medtronic, Inc. · Stent, iliac vein
  2 reports
• Abre™ AB9U20060090

  Medtronic, Inc. · Stent, iliac vein
  1 death2 reports
• Abre™ AB9U20150090

  Medtronic, Inc. · Stent, iliac vein
  2 reports
• VICI VENOUS STENT ® SYSTEM H74912060100

  Veniti Inc · Stent, iliac vein
  2 reports
• Zilver Vena G57437

  Cook Ireland Ltd · Stent, iliac vein
  2 reports
• Zilver Vena G57438

  Cook Ireland Ltd · Stent, iliac vein
  2 reports
• Zilver Vena G57443

  Cook Ireland Ltd · Stent, iliac vein
  2 reports
• Zilver Vena G57444

  Cook Ireland Ltd · Stent, iliac vein
  2 reports
• Abre™ AB9U10040090

  Medtronic, Inc. · Stent, iliac vein
  1 report
• Abre™ AB9U10060090

  Medtronic, Inc. · Stent, iliac vein
  1 report
• Abre™ AB9U10080090

  Medtronic, Inc. · Stent, iliac vein
  1 report
• Abre™ AB9U20100090

  Medtronic, Inc. · Stent, iliac vein
  1 report
• Abre™ AB9U20120090

  Medtronic, Inc. · Stent, iliac vein
  1 report
• VENOUS WALLSTENT™ H74912044106870

  Boston Scientific Corporation · Stent, iliac vein
  1 report
• VENOUS WALLSTENT™ H74912044149070

  Boston Scientific Corporation · Stent, iliac vein
  1 report
• VENOUS WALLSTENT™ H74912044164070

  Boston Scientific Corporation · Stent, iliac vein
  1 report
• Zilver Vena G57433

  Cook Ireland Ltd · Stent, iliac vein
  1 report
• Zilver Vena G57435

  Cook Ireland Ltd · Stent, iliac vein
  1 report
• Zilver Vena G57439

  Cook Ireland Ltd · Stent, iliac vein
  1 report
• Zilver Vena G57441

  Cook Ireland Ltd · Stent, iliac vein
  1 report
• Zilver Vena G57442

  Cook Ireland Ltd · Stent, iliac vein
  1 report