Gemini 220 XP

FDA registration

DORNIER MEDTECH GMBH·1 product·🇩🇪 Germany

EXTRA CORPOREAL SHOCKWAVE LITHOTRIPTER

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

Lithotriptor, Extracorporeal Shock-Wave, Urological

FDA classification

FDA Class 2 ·Lithotriptor, Extracorporeal Shock-Wave, Urological

Inion FreedomScrew

FDA registration

INION OY·1 product·🇫🇮 Finland

ARTIFEX SOLUTIONS, LLC

FDA registration

ARTIFEX SOLUTIONS, LLC·1 product·🇺🇸 United States

STRUCTURE MEDICAL, LLC.

FDA registration

STRUCTURE MEDICAL, LLC.·1 product·🇺🇸 United States

Synergy Health Sterilisation UK Ltd

FDA registration

Synergy Health Sterilisation UK Ltd·1 product·🇬🇧 United Kingdom

ARCTIC BIOMATERIALS OY

FDA registration

ARCTIC BIOMATERIALS OY·1 product·🇫🇮 Finland

Reduct Headless Compression Screw System

FDA registration

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

Gammatom S.r.l.

FDA registration

Gammatom S.r.l.·1 product·🇮🇹 Italy

Vaupell Midwest Molding and Tooling

FDA registration

Vaupell Midwest Molding and Tooling·2 products·🇺🇸 United States

EasyScreen Gastrointestinal Parasite Detection Kit

FDA registration

GENETIC SIGNATURES LIMITED·2 products·🇦🇺 Australia

Neptune 2 Waste Management System

FDA registration

Viant Medical, Inc.·2 products·🇺🇸 United States

Advanced Scar & Wound Hydrogel

FDA registration

Oculus Technologies of Mexico, S.A de C.V.·1 product·🇲🇽 Mexico

SANICURE BV

FDA registration

SANICURE BV·2 products·🇳🇱 Netherlands

TARGET DETACHABLE COIL

FDA 510(k)

FDA Class 2 ·Neurology

HEADLESS COMPRESSION SCREW

FDA 510(k)

FDA Class 2 ·Orthopedic

Device, Neurovascular Embolization

FDA classification

FDA Class 2 ·Device, Neurovascular Embolization

Screw, Fixation, Bone

FDA classification

FDA Class 2 ·Screw, Fixation, Bone