NeoStar Triple Lumen Catheter

FDA registration

STERILIZATION SERVICES OF GEORGIA, INC.·1 product·🇺🇸 United States

RIGHT ATRIAL CATHETER

FDA 510(k)

FDA Class 2 ·General Hospital

ZENEX Implant System_Narrow

FDA registration

IZENIMPLANT CO., LTD.·2 products·🇰🇷 South Korea

ZENEX Implant System_Narrow

FDA registration

IZENIMPLANT CO., LTD.·2 products·🇰🇷 South Korea

Plateau Titanium System

FDA registration

LIFE SPINE·1 product·🇺🇸 United States

Intervertebral fusion device with bone graft, lumbar

FDA registration

Acero Precision·1 product·🇺🇸 United States

Tech-Medical Services

FDA registration

TECH MEDICAL SERVICES, INC.·1 product·🇺🇸 United States

Rapid Response Adenovirus Test Cassette

FDA registration

BTNX Inc.·1 product·🇨🇦 Canada

Anspach Compact SpeedReducer

FDA registration

SYNTHES GMBH·1 product·🇨🇭 Switzerland

Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

FDA classification

FDA Class 2 ·Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

PLATEAU SPACER SYSTEM TITANIUM

FDA 510(k)

FDA Class 2 ·Orthopedic

EDWARDS DIRECTIONAL CATHETER

FDA 510(k)

FDA Class 2 ·Cardiovascular

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

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

Catheter, Percutaneous

FDA classification

FDA Class 2 ·Catheter, Percutaneous