Injector, vertebroplasty (does not contain cement)

FDA product code OAR · Class 1 · 15 devices · 95 reports · 6 devices named in recalls

• AVAflex 1025011500

  Stryker Corporation · Injector, vertebroplasty (does not contain cement)
  1 recall9 reports
• DFINE® 00884450374375

  Merit Medical Systems, Inc. · Injector, vertebroplasty (does not contain cement)
  1 recall0 reports
• DFINE® 00884450374399

  Merit Medical Systems, Inc. · Injector, vertebroplasty (does not contain cement)
  1 recall0 reports
• StabiliT TOUCH™ Syringe 00884450662144

  Merit Medical Systems, Inc. · Injector, vertebroplasty (does not contain cement)
  1 recall0 reports
• PCD 0506485000

  Stryker Corporation · Injector, vertebroplasty (does not contain cement)
  1 recall0 reports
• VertePort 0306511000

  Stryker Corporation · Injector, vertebroplasty (does not contain cement)
  1 recall0 reports
• iVAS 0306330000

  Stryker Corporation · Injector, vertebroplasty (does not contain cement)
  41 reports
• VERTECEM II 03.702.215S

  Synthes GmbH · Injector, vertebroplasty (does not contain cement)
  22 reports
• AVAflex 1025011000

  Stryker Corporation · Injector, vertebroplasty (does not contain cement)
  11 reports
• NA 0306110000

  Stryker Corporation · Injector, vertebroplasty (does not contain cement)
  3 reports
• iVAS 0306530000

  Stryker Corporation · Injector, vertebroplasty (does not contain cement)
  3 reports
• NA 0306130000

  Stryker Corporation · Injector, vertebroplasty (does not contain cement)
  2 reports
• VertePort 0306410000

  Stryker Corporation · Injector, vertebroplasty (does not contain cement)
  2 reports
• NA 0306131000

  Stryker Corporation · Injector, vertebroplasty (does not contain cement)
  1 report
• BIOPSYBELL EASYNJECT

  Biopsybell Srl · Injector, Vertebroplasty (Does Not Contain Cement)
  1 report