21 results · 44ms · Sources: EU EUDAMED, US FDA

Heli-FX EndoAnchor System

FDA registration
Medtronic Distribution Center·1 product·🇺🇸 United States

Heli-FX EndoAnchor System

FDA registration
MEDTRONIC IRELAND·1 product·🇮🇪 Ireland

Heli-FX EndoAnchor System

FDA registration
MEDTRONIC PERFUSION SYSTEMS·1 product·🇺🇸 United States

Synergy Health Ireland Ltd

FDA registration
Synergy Health Ireland Ltd·1 product·🇮🇪 Ireland

Heli-FX EndoAnchor System

FDA registration
Medtronic Vascular·1 product·🇺🇸 United States

Heli-FX EndoAnchor System

FDA 510(k)
FDA Class 2 ·Cardiovascular

Endovascular Suturing System

FDA classification
FDA Class 2 ·Endovascular Suturing System

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

17G Wallace Dual Lumen

FDA registration
COOPERSURGICAL, INC.·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

KAWASUMI LABORATORIES AMERICA, INC.

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

CUTTING EDGE SPINE INTERBODY FUSION DEVICE

FDA 510(k)
FDA Class 2 ·Orthopedic

NON-STERILE, POWDER FREE NITRILE EXAMINATION GLOVE, BLUE COLOR, POLYMER COATED, TESTED WITH CHEMOTHERAPY DRUGS

FDA 510(k)
FDA Class 1 ·General Hospital

Intervertebral Fusion Device With Bone Graft, Lumbar

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