K2M Patient Specific Rods

FDA registration

K2M, INC.·3 products·🇺🇸 United States

K2M Patient Specific Rods

FDA 510(k)

FDA Class 2 ·Orthopedic

FUKUSHIMA SUCTION TUBE

FDA UDI

SONTEC INSTRUMENTS, INC.·00192896009691·FUKUSHIMA SUCTION TUBE

FUKUSHIMA SUCTION TUBE

FDA UDI

SONTEC INSTRUMENTS, INC.·B0991803760·FUKUSHIMA SUCTION TUBE

PE-210A

FDA registration

Nihon Kohden Corporation - Eastern Japan Logistics Center·2 products·🇯🇵 Japan

PE-210A

FDA registration

NIHON KOHDEN CORP.·2 products·🇯🇵 Japan

PE-210A

FDA registration

NIHON KOHDEN TOMIOKA PRODUCTION CENTER·2 products·🇯🇵 Japan

NanoKnife

FDA registration

Sterigenics U.S., LLC·1 product·🇺🇸 United States

PE-210A

FDA registration

NIHON KOHDEN AMERICA, INC.·2 products·🇺🇸 United States

PE-210A

FDA registration

Nihon Kohden Corporation - Tokorozawa establishment Advanced Technology Center·2 products·🇯🇵 Japan

PE-210A

FDA registration

Nihon Kohden Tomioka Corporation·2 products·🇯🇵 Japan

EVERON CENTRAL DISPLAY STATION - CDS, MODEL VERSION 1.0.0

FDA 510(k)

FDA Class 2 ·Cardiovascular

ONCOBIONIC SYSTEM

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Low Energy Direct Current Thermal Ablation System

FDA classification

FDA Class 2 ·Low Energy Direct Current Thermal Ablation System

Thoracolumbosacral Pedicle Screw System

FDA classification

FDA Class 2 ·Thoracolumbosacral Pedicle Screw System

System, Network And Communication, Physiological Monitors

FDA classification

FDA Class 2 ·System, Network And Communication, Physiological Monitors