Endoskeleton® TAS Interbody Fusion Device

FDA registration

Titan Spine, a Division of Medtronic·3 products·🇺🇸 United States

Endoskeleton® TAS Interbody Fusion Device

FDA registration

MEDTRONIC SOFAMOR DANEK USA, INC.·3 products·🇺🇸 United States

Endoskeleton® TAS Interbody Fusion Device

FDA registration

Medtronic Engineering and Innovation Center (MEIC)·3 products·🇮🇳 India

Endoskeleton® TAS Interbody Fusion Device

FDA registration

MEDTRONIC SOFAMOR DANEK USA, INC.·3 products·🇺🇸 United States

Sterigenics US LLC

FDA registration

Sterigenics US LLC·2 products·🇺🇸 United States

Endoskeleton® TAS Interbody Fusion Device, Endoskeleton® TAS Hyperlordotic Interbody Fusion Device and Endoskeleton® TCS Interbody Fusion Device

FDA 510(k)

FDA Class 2 ·Orthopedic

Infinix V

FDA registration

Canon Medical Systems Corporation·2 products·🇯🇵 Japan

BIOFOAM

FDA registration

WRIGHT MEDICAL TECHNOLOGY, INC.·2 products·🇺🇸 United States

BIOFOAM

FDA registration

WRIGHT MEDICAL TECHNOLOGY, INC.·2 products·🇺🇸 United States

DuraStat

FDA registration

DuraStat·1 product·🇺🇸 United States

Fourstar Group

FDA registration

Fourstar Group·1 product·🇭🇰 Hong Kong

PII / Candida species nucleic acid detection system

FDA registration

MONOCENT INC.·1 product·🇺🇸 United States

VACPLUS SUCTION UNIT

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

BIOFOAM BONE WEDGE

FDA 510(k)

FDA Class 2 ·Orthopedic

Intervertebral Fusion Device With Bone Graft, Cervical

FDA classification

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

Apparatus, Suction, Ward Use, Portable, Ac-Powered

FDA classification

FDA Class 2 ·Apparatus, Suction, Ward Use, Portable, Ac-Powered

Plate, Fixation, Bone

FDA classification

FDA Class 2 ·Plate, Fixation, Bone