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.

Howmedica Leibinger, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

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

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