PowerPort™ ClearVUE™ Slim Implantable Ports

FDA registration

C.R. BARD, INC.·1 product·🇺🇸 United States

PowerPort™ ClearVUE™ Slim Implantable Ports

FDA registration

BARD REYNOSA S.A. DE C.V.·1 product·🇲🇽 Mexico

PowerPort™ ClearVUE™ Slim Implantable Ports

FDA registration

Bard Access Systems, Inc.·1 product·🇺🇸 United States

PowerPort™ ClearVUE™ Slim Implantable Ports

FDA registration

C.R. BARD, INC.·1 product·🇺🇸 United States

PowerPort™ ClearVUE™ Slim Implantable Ports and PowerPort™ ClearVUE™ Slim Implantable Ports

FDA 510(k)

FDA Class 2 ·General Hospital

CoRoent

FDA UDI

Nuvasive, Inc.·00887517578945·CoRoent Ant TLIF Ti, 14x12x32mm 8°

Sklar®

FDA UDI

SKLAR CORPORATION·10649111137556·SCHUKNECHT WIRE CUT SCISS 4"

SOMATOM SPIRIT

FDA registration

SIEMENS SHANGHAI, MEDICAL EQUIPMENT LTD.·1 product·🇨🇳 China

nvc

FDA registration

NVISION BIOMEDICAL TECHNOLOGIES, INC·1 product·🇺🇸 United States

Intervertebral Body Fusion Device

FDA registration

MEDICAL DEVICE AND IMPLANTS LLC·1 product·🇺🇸 United States

Maestro system

FDA registration

MOON SURGICAL, INC.·1 product·🇺🇸 United States

eXciteOSA, Neuromuscular tongue muscle stimulator for the reduction of snoring and obstructive sleep apnea

FDA registration

MILLI-HENRY ELECTRONICS CO., LTD.·1 product·🇨🇳 China

GripTract-GI Endoscopic Tissue Manipulator

FDA registration

ACTUATED MEDICAL, INC.·1 product·🇺🇸 United States

Port & Catheter, Implanted, Subcutaneous, Intravascular

FDA classification

FDA Class 2 ·Port & Catheter, Implanted, Subcutaneous, Intravascular

SOMATOM SPIRIT

FDA 510(k)

FDA Class 2 ·Radiology

nvc

FDA 510(k)

FDA Class 2 ·Orthopedic

Intervertebral Fusion Device With Bone Graft, Cervical

FDA classification

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

System, X-Ray, Tomography, Computed

FDA classification

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