NeoTell

FDA registration

NEOSS, LTD.·1 product·🇬🇧 United Kingdom

Beacon

FDA registration

OSSTELL AB·1 product·🇸🇪 Sweden

Osstell Beacon

FDA 510(k)

FDA Class 1 ·Dental

Handpiece, Direct Drive, Ac-Powered

FDA classification

FDA Class 1 ·Handpiece, Direct Drive, Ac-Powered

SCENARIA

FDA registration

FUJIFILM Healthcare Manufacturing Corporation Kashiwa Office·1 product·🇯🇵 Japan

JULIET

FDA registration

Alpes CN·1 product·🇫🇷 France

Synergy Health Daniken AG

FDA registration

Synergy Health Daniken AG·1 product·🇨🇭 Switzerland

COULOT DECOLLETAGE

FDA registration

COULOT DECOLLETAGE·1 product·🇫🇷 France

SCENARIA

FDA registration

FUJIFILM Corporation Medical Systems Research & Development Center Kashiwa·1 product·🇯🇵 Japan

JULIET

FDA registration

SPINEART SA·1 product·🇨🇭 Switzerland

CEFIMECA

FDA registration

CEFIMECA·1 product·🇫🇷 France

Scenaria

FDA registration

CENTURY YAMAKYU CORPORATION·1 product·🇯🇵 Japan

JULIET

FDA registration

ALPES CN SAS·1 product·🇫🇷 France

THE O R COMPANY PTY LTD

FDA registration

THE O R COMPANY PTY LTD·1 product·🇦🇺 Australia

Midline Navigation Screw Guide

FDA registration

Mighty Oak Medical·1 product·🇺🇸 United States

RUSCH ENDOBRONCHIAL TUBES

FDA registration

TASCO BERHAD·1 product·🇲🇾 Malaysia

DYNAMIK INTERVERTEBRAL BODY FUSION DEVICE

FDA 510(k)

FDA Class 2 ·Orthopedic

SCENARIA WHOLE-BODY X-RAY CT SYSTEM

FDA 510(k)

FDA Class 2 ·Radiology

System, X-Ray, Tomography, Computed

FDA classification

FDA Class 2 ·System, X-Ray, Tomography, Computed

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

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