Rampart One Lumbar Interbody Fusion Device

FDA registration

SPINEOLOGY INC.·1 product·🇺🇸 United States

Spineology5627 (LN) - Rampart One Lumbar Interbody Fusion System

FDA registration

Isomedix Operations, Inc.·1 product·🇺🇸 United States

Rampart One Lumbar Interbody Fusion Device

FDA 510(k)

FDA Class 2 ·Orthopedic

BIOMET HIP SYSTEM

FDA UDI

Biomet Orthopedics, LLC·00880304256668·

Biomet® Hip System

FDA UDI

Biomet Orthopedics, LLC·00887868308345·

Intervertebral Fusion Device With Integrated Fixation, Lumbar

FDA classification

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

Noble gloves

FDA registration

Clark Core Services, LLC·1 product·🇺🇸 United States

Synergy Health Allershausen GmbH

FDA registration

Synergy Health Allershausen GmbH·6 products·🇩🇪 Germany

Galvanic Spa, Model: SKB-1405

FDA registration

Shenzhen Siken 3D Technology Development Co., Ltd.·1 product·🇨🇳 China

ImmunoCAP Allergen, w1, Common ragweed

FDA registration

PHADIA US INC.·1 product·🇺🇸 United States

ImmunoCAP Allergen, w1, Common ragweed

FDA registration

PHADIA AB·1 product·🇸🇪 Sweden

NITRILE EXAMINATION GLOVES POLYMER COATED (WHITE, BLUE, AND BLACK COLOR)

FDA 510(k)

FDA Class 1 ·General Hospital

MODIFICATIONS TO CD HORIZON SPINAL SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

Thoracolumbosacral Pedicle Screw System

FDA classification

FDA Class 2 ·Thoracolumbosacral Pedicle Screw System

Polymer Patient Examination Glove

FDA classification

FDA Class 1 ·Polymer Patient Examination Glove