ReliOn Premier Lancing Device

FDA registration

ARKRAY Factory, Inc.·1 product·🇯🇵 Japan

ReliOn Premier Lancing Device

FDA registration

ARKRAY FACTORY USA, INC.·1 product·🇺🇸 United States

ReliOn Premier Lancing Device

FDA registration

ARKRAY, INC.·1 product·🇯🇵 Japan

Multi-Lancet Device 2

FDA registration

ARKRAY Industry West Inc.·1 product·🇵🇭 Philippines

Multi-Lancet Device 2, ReliOn Premier Lancing Device

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Multiple Use Blood Lancet For Single Patient Use Only

FDA classification

FDA Class 2 ·Multiple Use Blood Lancet For Single Patient Use Only

StealthStation Cranial Software v1.3

FDA registration

MEDTRONIC NAVIGATION, INC.·1 product·🇺🇸 United States

DynaCAD

FDA registration

Philips DS North America LLC·1 product·🇺🇸 United States

J & J INSTRUMENTS

FDA UDI

J & J INSTRUMENTS INC·00817524025507·OPERATING SCI 5.5"" B/B CVD

TriVerse Femoral Trial PS Insert

FDA UDI

SIGNATURE ORTHOPAEDICS PTY LTD·09348215097813·

Qraycam PRO

FDA registration

AIOBIO CO., LTD.·1 product·🇰🇷 South Korea

CureSight

FDA registration

NOVASIGHT·1 product·🇮🇱 Israel

AERONEB PROFESSIONAL NEBULIZER SYSTEM, MODEL#AG-AP6000

FDA 510(k)

FDA Class 2 ·Anesthesiology

FLASH PTA BALLON DILATATION CATHETER-5MM X 19MM X 135CM

FDA 510(k)

FDA Class 2 ·Cardiovascular

Catheter, Angioplasty, Peripheral, Transluminal

FDA classification

FDA Class 2 ·Catheter, Angioplasty, Peripheral, Transluminal

Nebulizer (Direct Patient Interface)

FDA classification

FDA Class 2 ·Nebulizer (Direct Patient Interface)