SyncVision Software Version 3.2

FDA registration

VOLCANO CORPORATION·1 product·🇺🇸 United States

SyncVision Software Version 3.2

FDA registration

Volcano Corporation·1 product·🇺🇸 United States

SyncVision System

FDA registration

DHL SUPPLY CHAIN (NETHERLANDS) B.V.·1 product·🇳🇱 Netherlands

SyncVision System

FDA 510(k)

FDA Class 2 ·Radiology

K151004

FDA registration

EXEL INC. DBA DHL SUPPLY CHAIN (USA)·1 product·🇺🇸 United States

Tasso+ Convenience Kit

FDA UDI

Tasso, Inc·00850038691042·

ProLift Lateral

FDA UDI

Life Spine, Inc.·00190837081591·

ALL PURPOSE CUFF

FDA registration

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

ARK Methotrexate Calibrator

FDA registration

ARK DIAGNOSTICS INC·3 products·🇺🇸 United States

ALL PURPOSE CUFF

FDA registration

SUNTECH MEDICAL DEVICES (SHENZHEN) CO., LTD.·1 product·🇨🇳 China

ADVIEW

FDA registration

AMERICAN DIAGNOSTIC CORP.·1 product·🇺🇸 United States

SunTech Cuff, All purpose general (Adult)

FDA registration

Baxter Healthcare - Tel Aviv·1 product·🇮🇱 Israel

Bausch & Lomb Incorporated

FDA registration

Bausch & Lomb Incorporated·1 product·🇺🇸 United States

8-04-15600, 1085 ICS Impulse (Lateral only Head Impulse System)

FDA registration

Natus Manufacturing Limited·1 product·🇮🇪 Ireland

8-04-15600, 1085 ICS Impulse (Lateral only Head Impulse System)

FDA registration

Natus Manufacturing Limited·1 product·🇮🇪 Ireland

Interventional Fluoroscopic X-Ray System

FDA classification

FDA Class 2 ·Interventional Fluoroscopic X-Ray System

SMARTXIDE 50 HS/MS

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

ALL PURPOSE CUFF, MODEL 222APC

FDA 510(k)

FDA Class 2 ·Cardiovascular

Blood Pressure Cuff

FDA classification

FDA Class 2 ·Blood Pressure Cuff

Powered Laser Surgical Instrument

FDA classification

FDA Class 2 ·Powered Laser Surgical Instrument