Instrument, Surgical, Non-Powered

FDA product code HAO · Class 1 · 18 devices · 29 reports · 1 devices named in recalls

• SenSight™ B31030

  Medtronic, Inc. · INSTRUMENT, SURGICAL, NON-POWERED
  1 recall7 reports
• WECK IPN006432

  Teleflex Incorporated · INSTRUMENT, SURGICAL, NON-POWERED
  3 reports
• NA 365538

  Medtronic, Inc. · INSTRUMENT, SURGICAL, NON-POWERED
  2 reports
• 3.3mm Mini-Bolt VUE 21133

  Monteris Medical Inc · INSTRUMENT, SURGICAL, NON-POWERED
  2 reports
• NA 1120

  Advanced Neuromodulation Systems, Inc. · INSTRUMENT, SURGICAL, NON-POWERED
  2 reports
• DBS™ 3755

  Medtronic, Inc. · INSTRUMENT, SURGICAL, NON-POWERED
  1 report
• SenSight™ B31030

  Medtronic, Inc. · INSTRUMENT, SURGICAL, NON-POWERED
  1 report
• Mini-Bolt System 21228

  Monteris Medical Inc · Instrument, Surgical, Non-Powered
  1 report
• AESCULAP FV002R

  Aesculap AG · INSTRUMENT, SURGICAL, NON-POWERED
  1 report
• Cyberonics® Tunneler Model 402

  Livanova USA, Inc. · Instrument, Surgical, Non-Powered
  1 report
• RELIANCE LITe 48060500

  Stryker Corporation · INSTRUMENT, SURGICAL, NON-POWERED
  1 report
• XIA 4.5 48130100

  Stryker Corporation · INSTRUMENT, SURGICAL, NON-POWERED
  1 report
• OASYS 48561039

  Stryker Corporation · INSTRUMENT, SURGICAL, NON-POWERED
  1 report
• Integra® Jarit® 285120

  Integra Lifesciences Production Corporation · INSTRUMENT, SURGICAL, NON-POWERED
  1 report
• NeuroBalloon™ 7CBD10

  Integra LifeSciences Switzerland Sàrl · INSTRUMENT, SURGICAL, NON-POWERED
  1 report
• Integra® Jarit® 285391

  Integra Lifesciences Production Corporation · INSTRUMENT, SURGICAL, NON-POWERED
  1 report
• V. Mueller NL1098

  Steris Corporation · INSTRUMENT, SURGICAL, NON-POWERED
  1 report
• WECK IPN028496

  Teleflex Incorporated · INSTRUMENT, SURGICAL, NON-POWERED
  1 report