PEEK Corpectomy

FDA registration

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

NuVasive® PEEK Corpectomy System

FDA registration

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

NuVasive PEEK Corpectomy System

FDA 510(k)

FDA Class 2 ·Orthopedic

HHM

FDA UDI

Oticon A/S·05707131279910·H160, DESIGNRITE 10 WL VLI HHM

Extra/Xtender & Sprint processor

FDA registration

MEDIVANCE INSTRUMENTS LTD.·1 product·🇬🇧 United Kingdom

RevoLix and R Jr

FDA registration

LISA LASER PRODUCTS GMBH·1 product·🇩🇪 Germany

ProLift Expandable Spacer System

FDA UDI

Life Spine, Inc.·00190837065744·

V. Mueller ESU

FDA registration

STERIS CORPORATION·1 product·🇺🇸 United States

STARband, STARlight

FDA registration

ORTHOMERICA PRODUCTS, INC.·2 products·🇺🇸 United States

BBraun11480 (MS) - B. Braun Surgical, S.A. (Dafilon)

FDA registration

Synergy Health Marseille SAS·1 product·🇫🇷 France

Spinal Vertebral Body Replacement Device

FDA classification

FDA Class 2 ·Spinal Vertebral Body Replacement Device

REVOLIX AND REVOLIX JR

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

XTENDER FILM PROCESSOR, SPRINT FILM PROCESSOR MODEL XTENDER MODEL SPRINT

FDA 510(k)

FDA Class 2 ·Radiology

Processor, Radiographic-Film, Automatic

FDA classification

FDA Class 2 ·Processor, Radiographic-Film, Automatic

Powered Laser Surgical Instrument

FDA classification

FDA Class 2 ·Powered Laser Surgical Instrument