LUQUE SEGMENTAL SPINAL INSTRUMENTATION

FDA registration

Sterigenics US, LLC·1 product·🇺🇸 United States

Luque Segmental Spinal Instrumentat

FDA registration

ZIMMER, INC.·1 product·🇺🇸 United States

Loops

FDA registration

FORT WAYNE METALS RESEARCH PRODUCTS, LLC·1 product·🇺🇸 United States

LUQUE SEGMENTAL SPINAL INSTRUMENTATION

FDA 510(k)

FDA Class 2 ·Orthopedic

GE Lightspeed 16 CT scanner

FDA registration

BAY SHORE MEDICAL EQUIPMENT, LLC·1 product·🇺🇸 United States

Olive Branch Distribution Center

FDA registration

Olive Branch Distribution Center·1 product·🇺🇸 United States

Highridge Medical, LLC

FDA registration

Highridge Medical, LLC·1 product·🇺🇸 United States

TM Ardis and Accessories

FDA registration

Zimmer Trabecular Metal Technology, Inc.·1 product·🇺🇸 United States

LightSpeed Ultra 16

FDA registration

GE HANGWEI MEDICAL SYSTEMS CO., LTD.·1 product·🇨🇳 China

HRFTK-ACT - Kaolin ACT Tubes

FDA registration

Accriva Diagnostics, Inc.·1 product·🇺🇸 United States

TM ARDIS INTERBODY SYSTEM TM ARDIS INTERBODY SYSTEM INSTRUMENATION

FDA 510(k)

FDA Class 2 ·Orthopedic

LIGHTSPEED 4.0 CT SCANNER SYSTEM

FDA 510(k)

FDA Class 2 ·Radiology

Appliance, Fixation, Spinal Interlaminal

FDA classification

FDA Class 2 ·Appliance, Fixation, Spinal Interlaminal

System, X-Ray, Tomography, Computed

FDA classification

FDA Class 2 ·System, X-Ray, Tomography, Computed

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar