MILLSTONE MEDICAL OUTSOURCING LLC.

FDA registration

MILLSTONE MEDICAL OUTSOURCING LLC.·4 products·🇺🇸 United States

Sterigenics US, LLC

FDA registration

Sterigenics US, LLC·4 products·🇺🇸 United States

NuVasive MOD-EX XLIF Interbody System, NuVasive MOD-EX XLIF Plated 2 Interbody System

FDA registration

NUVASIVE, INC.·4 products·🇺🇸 United States

ARCH Medical Solutions - Seabrook

FDA registration

ARCH Medical Solutions - Seabrook·4 products·🇺🇸 United States

ARCH Medical Solutions - Memphis

FDA registration

ARCH Medical Solutions - Memphis·4 products·🇺🇸 United States

Modulus

FDA registration

GLOBUS MEDICAL, INC.·4 products·🇺🇸 United States

ARCH Medical Solutions - Memphis

FDA registration

ARCH Medical Solutions - Memphis·4 products·🇺🇸 United States

NuVasive MOD-EX XLIF Interbody System, NuVasive MOD-EX XLIF Plated 2.0 Interbody System

FDA 510(k)

FDA Class 2 ·Orthopedic

Blade Scalpel

FDA UDI

KATENA PRODUCTS, INC.·00841668113547·SLIT BLADE 3.2MM ANGLED (BX/5)

Boston Scientific Corporation

FDA registration

Boston Scientific Corporation·2 products·🇨🇷 Costa Rica

Boston Scientific Limited

FDA registration

Boston Scientific Limited·2 products·🇮🇪 Ireland

BOSTON SCIENTIFIC CORPORATION

FDA registration

BOSTON SCIENTIFIC CORPORATION·2 products·🇺🇸 United States

Boston Scientific Corporation

FDA registration

Boston Scientific Corporation·2 products·🇺🇸 United States

Restore Robotics

FDA registration

RESTORE ROBOTICS REPAIRS LLC·2 products·🇺🇸 United States

Synergy Health AST, SRL

FDA registration

Synergy Health AST, SRL·2 products·🇨🇷 Costa Rica

Total Immunoglobulin E (IgE) - C22529

FDA registration

Beckman Coulter Ireland Inc·1 product·🇮🇪 Ireland

Disposable Non-invasive EEG Sensor

FDA registration

SHENZHEN MED-LINK ELECTRONICS TECH CO.,LTD·1 product·🇨🇳 China

Captivator Single-Use Polypectomy Snares, Captiflex Single-Use Polypectomy Snares

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

ELECTROMEDICARIN 900

FDA 510(k)

FDA Class 2 ·Physical Medicine

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

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