Medical Device Manufacturer · US , Rockville , MD

Walter Lorenz Surgical, Inc. - FDA 510(k) Cleared Devices

56 submissions · 56 cleared · Since 1986

Total

Cleared

Denied

Walter Lorenz Surgical, Inc. has 56 FDA 510(k) cleared medical devices. Based in Rockville, US.

Historical record: 56 cleared submissions from 1986 to 2007. Primary specialty: Dental.

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

FDA 510(k) Regulatory Record - Walter Lorenz Surgical, Inc.

56 devices

1-12 of 56

Cleared Feb 09, 2007

LORENZ ORTHODONTIC ANCHORAGE SYSTEM

K063386 · OAT

Dental · 93d

Cleared Jan 12, 2007

LORENZ TITANIUM FRACTURE / RECONSTRUCTION DEVICES AND PRE-BENT PLATES

K063052 · JEY

Dental · 100d

Cleared Dec 18, 2006

LORENZ STERNAL CLOSURE SYSTEM

LORENZ PECTUS SUPPORT BAR, TITANIUM

Ear, Nose, Throat · 53d

Cleared May 14, 2004

LORENZ RESORBABLE DISTRACTION SYSTEM OR EXPANDER

K030425 · JEY

Dental · 459d

Cleared May 13, 2004

MODIFICATION TO SELF-DRILLING RADIOGRAPHIC MARKERS

K040990 · NEU

General & Plastic Surgery · 27d

Cleared May 05, 2004

LORENZ SELF-DRILLING IMF SCREW

K040983 · DZE

Dental · 20d

Cleared Dec 15, 2003

LORENZ STERNAL CLOSURE SYSTEM

K033740 · HWC

Orthopedic · 17d

Cleared Aug 11, 2003

LORENZ 2.4 SELF DRILLING SCREWS

K032228 · HWC

Orthopedic · 21d

Cleared Jun 26, 2003

RAPIDFIRE SELF DRILLING SCREWS

K031751 · HWC

Orthopedic · 21d

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Walter Lorenz Surgical, Inc. - FDA 510(k) Cleared Devices

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