Intervertebral fusion device with bone graft, lumbar

FDA registration

ALTUS PARTNERS·1 product·🇺🇸 United States

Intervertebral fusion device with bone graft, lumbar

FDA registration

Acero Precision·1 product·🇺🇸 United States

Altus Spine Interbody Fusion System

FDA 510(k)

FDA Class 2 ·Orthopedic

Treasure Floppy

FDA registration

ASAHI INTECC CO., LTD.·1 product·🇯🇵 Japan

Treasure Floppy

FDA registration

ASAHI INTECC (THAILAND) CO., LTD.·1 product·🇹🇭 Thailand

Treasure Floppy

FDA registration

ASAHI INTECC HANOI CO., LTD.·1 product·🇻🇳 Vietnam

Absoclear

FDA registration

PHARMAPLAST S.A.E.·1 product·🇪🇬 Egypt

JOLIFE AB

FDA registration

JOLIFE AB·1 product·🇸🇪 Sweden

ASAHI TREASURE FLOPPY PERIPHERAL GUIDE WIRE

FDA 510(k)

FDA Class 2 ·Cardiovascular

BLOOD PRESSURE METER MODEL CH-101

FDA 510(k)

FDA Class 2 ·Cardiovascular

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

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

Wire, Guide, Catheter

FDA classification

FDA Class 2 ·Wire, Guide, Catheter

System, Measurement, Blood-Pressure, Non-Invasive

FDA classification

FDA Class 2 ·System, Measurement, Blood-Pressure, Non-Invasive