VivoSight

FDA registration

MICHELSON DIAGNOSTICS LTD·1 product·🇬🇧 United Kingdom

VIVOSIGHT TOPICAL OCT SYSTEM

FDA 510(k)

FDA Class 2 ·Radiology

System, Imaging, Optical Coherence Tomography (Oct)

FDA classification

FDA Class 2 ·System, Imaging, Optical Coherence Tomography (Oct)

APEX Knee System

FDA UDI

Omni Life Science, Inc.·00841690198369·AK3 PS Insert Trial Size 5, 20mm

EMG

FDA registration

EMG TECHNOLOGY CO., LTD.·1 product·🇹🇼 Taiwan

Bluephase G2

FDA registration

Ivoclar Vivadent GmbH·1 product·🇩🇪 Germany

Fiber Optic Rod

FDA registration

SCHOTT CR, S.R.O.·1 product·🇨🇿 Czechia

Bluephase G2

FDA registration

IVOCLAR VIVADENT AG·1 product·🇱🇮 Liechtenstein

Bluephase G2

FDA registration

IVOCLAR VIVADENT, INC.·1 product·🇨🇦 Canada

Bluephase G2

FDA registration

IVOCLAR VIVADENT Manufacturing GmbH·1 product·🇦🇹 Austria

NORTH AMERICAN WHOLESALERS LLC

FDA registration

NORTH AMERICAN WHOLESALERS LLC·1 product·🇺🇸 United States

EEKAY LOGISTICS LLC

FDA registration

EEKAY LOGISTICS LLC·1 product·🇺🇸 United States

Saneck Safety

FDA registration

The Cannon Group Inc·1 product·🇺🇸 United States

LumenVu Catheter Guidance System

FDA registration

FUJIFILM SONOSITE,INC.·1 product·🇺🇸 United States

BLUEPHASE

FDA 510(k)

FDA Class 2 ·Dental

NEXAN SYSTEM, MODEL NX-300

FDA 510(k)

FDA Class 2 ·Cardiovascular

Electrocardiograph, Ambulatory (Without Analysis)

FDA classification

FDA Class 2 ·Electrocardiograph, Ambulatory (Without Analysis)

Activator, Ultraviolet, For Polymerization

FDA classification

FDA Class 2 ·Activator, Ultraviolet, For Polymerization