NuVasive® MLX™ - Medial Lateral Expandable Lumbar Interbody System, NuVasive® AP Expandable XLIF System

FDA registration

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

ARCH Medical Solutions - Olive Branch

FDA registration

ARCH Medical Solutions - Olive Branch·1 product·🇺🇸 United States

MLX

FDA registration

GLOBUS MEDICAL, INC.·1 product·🇺🇸 United States

NuVasive MLX-Medial Lateral Expandable Lumbar Interbody System, NuVasive AP Expandable XLIF System

FDA 510(k)

FDA Class 2 ·Orthopedic

Z1

FDA registration

BREAS MEDICAL, INC.·1 product·🇺🇸 United States

Tempus

FDA registration

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

Light Sources General Sunlamp Series

FDA registration

LIGHT SOURCES, INC.·1 product·🇺🇸 United States

NRFit Syinge

FDA registration

JIANGSU CAINA MEDICAL CO., LTD·1 product·🇨🇳 China

CARDIODRIVE CATHETER ADVANCEMENT SYSTEM

FDA 510(k)

FDA Class 2 ·Cardiovascular

AAXTER A3 POSTERIOR SPINAL SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

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

Orthosis, Spondylolisthesis Spinal Fixation

FDA classification

FDA Class 2 ·Orthosis, Spondylolisthesis Spinal Fixation

Wire, Guide, Catheter

FDA classification

FDA Class 2 ·Wire, Guide, Catheter