Bi-Articular II Hip Device

FDA registration

Sterigenics US, LLC·1 product·🇺🇸 United States

Bi-Articular II Hip Device

FDA registration

ZIMMER, INC.·1 product·🇺🇸 United States

BI-ARTICULAR II HIP DEVICE

FDA 510(k)

FDA Class 2 ·Orthopedic

Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented

FDA classification

FDA Class 2 ·Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented

GC Initial™

FDA UDI

Gc America Inc.·15400556709099·GC Initial™ PC Pellets Bleached BO, 5pcs. X 2

GC Initial™

FDA UDI

Gc America Inc.·J0228720191·GC Initial™ PC Pellets Bleached BO, 5pcs. X 2

Gladstone ALIF Cage

FDA registration

SIGNATURE ORTHOPAEDICS PTY LIMITED·1 product·🇦🇺 Australia

Suture Removal Tray

FDA registration

Euroband Bioline LTD.·1 product·🇮🇱 Israel

ASI Staph Test

FDA registration

ARLINGTON SCIENTIFIC, INC.·1 product·🇺🇸 United States

Brisbane ALIF Device, Gladstone ALIF Device

FDA 510(k)

FDA Class 2 ·Orthopedic

AKITA2 APIXNEB

FDA 510(k)

FDA Class 2 ·Anesthesiology

Intervertebral Fusion Device With Integrated Fixation, Lumbar

FDA classification

FDA Class 2 ·Intervertebral Fusion Device With Integrated Fixation, Lumbar

Nebulizer (Direct Patient Interface)

FDA classification

FDA Class 2 ·Nebulizer (Direct Patient Interface)