Howmedica Leibinger, Inc.
Howmedica Leibinger, Inc. holds FDA 510(k) medical device clearances, first cleared 1996, most recent 1997.
Top product codes for Howmedica Leibinger, Inc.
Recent clearances by Howmedica Leibinger, Inc.
- K970912 — LEIBINGER SELF-DRILLING SCREW
- K972154 — COHEN DISTRACTOR
- K972166 — GUERRERO - BELL DISTRACTOR
- K961719 — EPITEC TITANIUM IMPLANT SYSTEM FOR THE SURGICAL ANCHORING OF FACIAL PROSTHESES
- K963030 — LEIBINGER IMF SCREW
- K970911 — LEE PLATE
- K963741 — LEIBINGER LUHR SMALL CRANIOMAXILLOFACIAL BONE SCREWS
- K964649 — VAZQUEZ DINER INTRAORAL DISTRACTION DEVICE
- K963739 — LEIBINGER - LUHR SMALL ORTHOPEDIC BONE SCREWS
- K963740 — LEIBINGER - LUHR SMALL MANDIBULAR BONE SCREWS
- K961120 — MARKER SYSTEM FOR STEREOTAXIC NAVIGATION
Data sourced from openFDA. This site is unofficial and independent of the FDA.