CoRoent XL-F System

FDA registration

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

CoRoent

FDA registration

NuVasive Manufacturing, LLC·1 product·🇺🇸 United States

CoRoent

FDA registration

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

COROENT XL-F SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

Oticon

FDA UDI

Oticon A/S·05707131270290·H11, DESIGNRITE 10 WL TC

Intervertebral Fusion Device With Integrated Fixation, Lumbar

FDA classification

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

ILIZAROV

FDA registration

Smith & Nephew, Inc.·1 product·🇺🇸 United States

BOSTON SCIENTIFIC CORPORATION

FDA registration

BOSTON SCIENTIFIC CORPORATION·1 product·🇨🇷 Costa Rica

ILIZAROV

FDA registration

SMITH & NEPHEW, INC.·1 product·🇺🇸 United States

ILIZAROV

FDA registration

Smith & Nephew, Inc.·1 product·🇺🇸 United States

Boston Scientific Limited

FDA registration

Boston Scientific Limited·1 product·🇮🇪 Ireland

Boston Scientific Corporation

FDA registration

Boston Scientific Corporation·1 product·🇺🇸 United States

ILIZAROV

FDA registration

Smith & Nephew, Inc.·1 product·🇺🇸 United States

ILIZAROV

FDA registration

Smith & Nephew, Inc.·1 product·🇺🇸 United States

Plastic Eye Wash Cup: EzyDose, Flents; 68354, HK68354, 68354CA

FDA registration

APOTHECARY PRODUCTS, LLC.·1 product·🇺🇸 United States

PEDIATRIC ENERGY REDUCER, MODELS AED-10 AND AED-20

FDA 510(k)

FDA Class 3 ·Cardiovascular

PARALLAX CONTOUR VERTEBRAL AUGMENTATION DEVICE

FDA 510(k)

FDA Class 2 ·Orthopedic

Cement, Bone, Vertebroplasty

FDA classification

FDA Class 2 ·Cement, Bone, Vertebroplasty

Automated External Defibrillators (Non-Wearable)

FDA classification

FDA Class 3 ·Automated External Defibrillators (Non-Wearable)