Leibinger - Luhr Small Orthopedic Bone Screws

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K963739 ↗

FDA Product Code

HWC

Device Class

Class II

Regulation

21 CFR Part 888.3040

Advisory Committee

Orthopedic

FDA Decision

SN

• Marker System for Stereotaxic Navigation

  Class II

  FDA 510(k) K961120 Active Cleared 10 May 1996

• Cohen Distractor

  Class II

  FDA 510(k) K972154 Active Cleared 11 Aug 1997

• Epitec Titanium Implant System for the Surgical Anchoring of Facial Prostheses

  Class II

  FDA 510(k) K961719 Active Cleared 17 Jul 1997

• Leibinger Imf Screw

  Class II

  FDA 510(k) K963030 Active Cleared 11 Apr 1997

• Leibinger - Luhr Small Mandibular Bone Screws

  Class II

  FDA 510(k) K963740 Active Cleared 28 Oct 1996

• Leibinger Self-Drilling Screw

  Class II

  FDA 510(k) K970912 Active Cleared 1 Oct 1997

See all devices from Howmedica Leibinger, Inc. →