Lorenz External Mandibular Distractor

No FDA recalls on record, checked 11 Oct 2026.

510(k) Number

K992873 ↗

FDA Product Code

MQN

Device Class

Class II

Regulation

21 CFR Part 872.4760

Advisory Committee

Dental

FDA Decision

SESE Substantially Equivalent

• Lorenz 1.0 Mm System

  Class II

  FDA 510(k) K922741 Active Cleared 23 Dec 1992

• Lorenz 1.5 X 4 Mm Lactosorb Tap Free Screw

  Class II

  FDA 510(k) K021522 Active Cleared 21 May 2002

• Steinhauser Titanium Mini Bone Plates & Screws

  Class II

  FDA 510(k) K862482 Active Cleared 25 Jul 1986

• Lorenz Pectus Support Bar

  Class II

  FDA 510(k) K972420 Active Cleared 11 Aug 1997

• Lorenz Maxilla (Le Fort) Distraction System

  Class II

  FDA 510(k) K982604 Active Cleared 23 Oct 1998

• Lumenon Xenon Light Source

  Class II

  FDA 510(k) K992050 Active Cleared 14 Sep 1999

See all devices from Walter Lorenz Surgical, Inc. →