Medical Device Manufacturer · US , Dallas , TX

Howmedica Leibinger, Inc. - FDA 510(k) Cleared Devices

11 submissions · 10 cleared · Since 1996

Total

Cleared

Denied

Howmedica Leibinger, Inc. has 10 FDA 510(k) cleared medical devices. Based in Dallas, US.

Historical record: 10 cleared submissions from 1996 to 1997. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Howmedica Leibinger, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Howmedica Leibinger, Inc.

11 devices

1-11 of 11

Cleared Oct 01, 1997

LEIBINGER SELF-DRILLING SCREW

GUERRERO - BELL DISTRACTOR

K972166 · JEY

Dental · 63d

Cleared Jul 17, 1997

EPITEC TITANIUM IMPLANT SYSTEM FOR THE SURGICAL ANCHORING OF FACIAL PROSTHESES

LEIBINGER LUHR SMALL CRANIOMAXILLOFACIAL BONE SCREWS

K963741 · HRS

Orthopedic · 142d

Cleared Jan 24, 1997

VAZQUEZ DINER INTRAORAL DISTRACTION DEVICE

K964649 · JEY

Dental · 65d

Cleared Jan 22, 1997

LEIBINGER - LUHR SMALL ORTHOPEDIC BONE SCREWS

K963739 · HWC

Orthopedic · 127d

Cleared Oct 28, 1996

LEIBINGER - LUHR SMALL MANDIBULAR BONE SCREWS

K963740 · JEY

Dental · 41d

Cleared May 10, 1996

MARKER SYSTEM FOR STEREOTAXIC NAVIGATION

K961120 · HAW

Neurology · 50d

Howmedica Leibinger, Inc. - FDA 510(k) Cleared Devices

Filters