HORIZON® Therapy System

FDA registration

THE MAGSTIM COMPANY LTD.·1 product·🇬🇧 United Kingdom

HORIZON Therapy System

FDA 510(k)

FDA Class 2 ·Neurology

Transcranial Magnetic Stimulator

FDA classification

FDA Class 2 ·Transcranial Magnetic Stimulator

NA

FDA UDI

KEY SURGICAL, INC.·00849771052296·K-Wire and Steinmann Pin Dispensers, No Dispen...

Lincotek Medical LLC

FDA registration

Lincotek Medical LLC·1 product·🇺🇸 United States

SteripackPoland (RB) - AVS A-LAT PEEK SPACERS, MODELS 48750XXX, 48751XXX, 48752XXX, 48753XXX

FDA registration

Synergy Health Radeberg GMBH·1 product·🇩🇪 Germany

Solta Medical, Inc.

FDA registration

Solta Medical, Inc.·1 product·🇺🇸 United States

ARIA DILATOR 14.5MM NM

FDA registration

STERIPACK MEDICAL POLAND SP. Z O.O.·1 product·🇵🇱 Poland

Advance Serenity® 14 Hydrophilic PTA Balloon Dilatation Catheter

FDA registration

Creagh Medical Ltd.·1 product·🇮🇪 Ireland

FRAXEL III SR LASER SYSTEM AND ACCESSORIES

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

AVS A-LAT PEEK SPACERS, MODELS 48750XXX, 48751XXX, 48752XXX, 48753XXX

FDA 510(k)

FDA Class 2 ·Orthopedic

Stablecut®

FDA UDI

ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024495401·

Stablecut®

FDA UDI

ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024495418·

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

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

Powered Laser Surgical Instrument

FDA classification

FDA Class 2 ·Powered Laser Surgical Instrument