Small tip kit

FDA registration

Natus Medical Denmark ApS·1 product·🇩🇰 Denmark

Type 1077 - MADSEN Aipha OAE+

FDA registration

Natus Manufacturing Limited·1 product·🇮🇪 Ireland

MADSEN ACCUSCREEN TYPE 1077

FDA 510(k)

FDA Class 2 ·Neurology

Stimulator, Auditory, Evoked Response

FDA classification

FDA Class 2 ·Stimulator, Auditory, Evoked Response

Hi-Torque Powerturn Guide Wires

FDA registration

ABBOTT VASCULAR·1 product·🇺🇸 United States

ROMD, LLC

FDA registration

ROMD, LLC·1 product·🇺🇸 United States

EVOL Lumbar Interbody System

FDA registration

CUTTING EDGE SPINE·1 product·🇺🇸 United States

wire, guide, catheter HT POWERTURN Guide Wires (includes POWERTURN ULTRA and FLEX)

FDA registration

Sterigenics Radiation Technologies, LLC·1 product·🇺🇸 United States

Hi-Torque Powerturn Guide Wires

FDA registration

Abbott Vascular Netherlands·1 product·🇳🇱 Netherlands

Hi-Torque Powerturn Guide Wires

FDA registration

ABBOTT VASCULAR·1 product·🇺🇸 United States

SB-KAWASUMI LABORATORIES, INC.

FDA registration

SB-KAWASUMI LABORATORIES, INC.·3 products·🇯🇵 Japan

KAWASUMI LABORATORIES (THAILAND) CO., LTD.

FDA registration

KAWASUMI LABORATORIES (THAILAND) CO., LTD.·3 products·🇹🇭 Thailand

Pneupac paraPAC plus

FDA registration

ICU Medical Czech Republic a. s.·2 products·🇨🇿 Czechia

KAWASUMI LABORATORIES AMERICA, INC.

FDA registration

KAWASUMI LABORATORIES AMERICA, INC.·3 products·🇺🇸 United States

Tidishield

FDA registration

VISIONFLEX PTY LIMITED·1 product·🇦🇺 Australia

CUTTING EDGE SPINE INTERBODY FUSION DEVICE

FDA 510(k)

FDA Class 2 ·Orthopedic

HI-TORQUE POWERTURN

FDA 510(k)

FDA Class 2 ·Cardiovascular

Wire, Guide, Catheter

FDA classification

FDA Class 2 ·Wire, Guide, Catheter

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

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