Toro-L Interbody Fusion System

FDA registration

INTEGRITY IMPLANTS INC.·2 products·🇺🇸 United States

ABLE MEDICAL DEVICES

FDA registration

ABLE MEDICAL DEVICES·1 product·🇺🇸 United States

Toro-L Interbody Fusion System

FDA 510(k)

FDA Class 2 ·Orthopedic

Oph. Cystotomes

FDA UDI

KATENA PRODUCTS, INC.·00841668113707·CYSTOTOME FORMED 23GA

Needle aspiration and injection

FDA UDI

KATENA PRODUCTS, INC.·00841668113639·RETROBULBAR NEEDLE 25GA 38MM

BIS Module

FDA registration

Philips North America LLC·4 products·🇺🇸 United States

BIS Module

FDA registration

Philips Medizin Systeme Boeblingen GmbH·4 products·🇩🇪 Germany

BIS Module

FDA registration

Philips North America LLC·4 products·🇺🇸 United States

DUET DRF

FDA registration

CMT MEDICAL TECHNOLOGIES, LTD.·2 products·🇮🇱 Israel

BIS Module

FDA registration

Philips Electronics Ltd·4 products·🇨🇦 Canada

Duet DRF

FDA registration

THALES AVS FRANCE SAS·2 products·🇫🇷 France

Synergy Health Ede BV

FDA registration

Synergy Health Ede BV·1 product·🇳🇱 Netherlands

CryoTreQ

FDA registration

VITREQ BV·1 product·🇳🇱 Netherlands

DUET DRF

FDA 510(k)

FDA Class 2 ·Radiology

AGILENT COMPONENT MONITORING SYSTEM, AGILENT V24/26, AGILENT BIS MODULE, MODEL M1175A/76A/77A,REV.L,M1205A,REV.L,M1034A

FDA 510(k)

FDA Class 2 ·Neurology

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

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

Index-Generating Electroencephalograph Software

FDA classification

FDA Class 2 ·Index-Generating Electroencephalograph Software

System, X-Ray, Fluoroscopic, Image-Intensified

FDA classification

FDA Class 2 ·System, X-Ray, Fluoroscopic, Image-Intensified