Bit, Drill

FDA product code HTW · Class 1 · 516 devices · 9,413 reports · 1 deaths reported · 16 devices named in recalls

• NA 03.133.102S

  Synthes GmbH · BIT, DRILL
  1 report
• NA 03.233.002

  Synthes GmbH · BIT, DRILL
  1 report
• NA 03.043.015

  Synthes GmbH · BIT, DRILL
  1 report
• NA 03.420.151

  Synthes GmbH · BIT, DRILL
  1 report
• NA 03.424.182

  Synthes GmbH · BIT, DRILL
  1 report
• NA 03.527.203

  Synthes GmbH · BIT, DRILL
  1 report
• NA 03.501.070

  Synthes GmbH · BIT, DRILL
  1 report
• NA 316.447

  Synthes GmbH · BIT, DRILL
  1 report
• NA KOMKM166-00-01

  Sterilmed, Inc. · BIT, DRILL
  1 report
• NA KOMKM166-310-19

  Sterilmed, Inc. · BIT, DRILL
  1 report
• NA SYN310.430

  Sterilmed, Inc. · BIT, DRILL
  1 report
• NA SYN310.510

  Sterilmed, Inc. · BIT, DRILL
  1 report
• NA SYN324.210

  Sterilmed, Inc. · BIT, DRILL
  1 report
• Admiral AP2-100312

  Seaspine Orthopedics Corporation · BIT, DRILL
  1 report
• Admiral AP2-100314

  Seaspine Orthopedics Corporation · BIT, DRILL
  1 report
• Irix-C Cervical Integrated Fusion System T066-0093

  Xtant Medical Holdings, Inc. · BIT, DRILL
  1 report