Restore Cervical Interbody Fusion

FDA registration

REPUBLIC SPINE·1 product·🇺🇸 United States

SURGICAL INSTRUMENT MANUFACTURERS, LLC

FDA registration

SURGICAL INSTRUMENT MANUFACTURERS, LLC·1 product·🇺🇸 United States

Republic Spine Restore Cervical Interbody Fusion System

FDA 510(k)

FDA Class 2 ·Orthopedic

Flex-Gar

FDA registration

ASIATIC FIBER CORPORATION·1 product·🇹🇼 Taiwan

ENDOSKELETON TC

FDA registration

Medtronic Engineering and Innovation Center (MEIC)·1 product·🇮🇳 India

ENDOSKELETON TC

FDA registration

MEDTRONIC SOFAMOR DANEK USA, INC.·1 product·🇺🇸 United States

Endoskeleton TC IBD

FDA registration

PERRYMAN COMPANY·1 product·🇺🇸 United States

Flex-Gar Sleeve

FDA registration

EMSI·1 product·🇺🇸 United States

ENDOSKELETON TC

FDA registration

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

Sterigenics US LLC

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

ENDOSKELETON TC

FDA registration

MEDTRONIC SOFAMOR DANEK USA, INC.·1 product·🇺🇸 United States

ENDOSKELETON TC

FDA registration

Titan Spine, a Division of Medtronic·1 product·🇺🇸 United States

Cochlear OsiaTM System

FDA registration

Cochlear Malaysia Sdn Bhd·1 product·🇲🇾 Malaysia

BIB Stent Placement Catheter

FDA registration

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

Cochlear OsiaTM System

FDA registration

Cochlear Limited - Brisbane·1 product·🇦🇺 Australia

Karma® Fixation System

FDA registration

SPINAL ELEMENTS, INC.·1 product·🇺🇸 United States

ENDOSKELETON TC

FDA 510(k)

FDA Class 2 ·Orthopedic

EMSI GARMENT ELECTRODES

FDA 510(k)

FDA Class 2 ·Neurology

Intervertebral Fusion Device With Bone Graft, Cervical

FDA classification

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

Electrode, Cutaneous

FDA classification

FDA Class 2 ·Electrode, Cutaneous