Renasys EZ PLUS

FDA registration

Smith & Nephew, Inc.·1 product·🇺🇸 United States

MODIFICATION TO RENASYS EZ PLUS NEGATIVE PRESSURE WOUND THERAPY

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Preat

FDA UDI

Preat Corporation·00842092175569·Preci Post Kit. Kit contains:. 25 Yellow transp...

Veronail Titanium Trochanteric Nail

FDA UDI

ORTHOFIX SRL·18032568868753·GRADUATED DRILL BIT D.4,8 L 330MM

Negative Pressure Wound Therapy Powered Suction Pump

FDA classification

FDA Class 2 ·Negative Pressure Wound Therapy Powered Suction Pump

Breeze Sleepgear with Dreamseal

FDA registration

Covidien·1 product·🇲🇽 Mexico

Breeze Sleepgear with Dreamseal

FDA registration

Covidien·1 product·🇲🇽 Mexico

SmartScrew® II

FDA registration

BBF STERILISATIONSSERVICE GMBH·2 products·🇩🇪 Germany

Breeze Sleepgear with Dreamseal

FDA registration

COVIDIEN·1 product·🇺🇸 United States

OsteoMed

FDA UDI

OSTEOMED LLC·00845694002325·90 x 90 x .6mm Mini, Formable Mesh Plate

Fiber Optic Illuminator

FDA UDI

I-TEK MEDICAL SOLUTIONS, INC.·00869836000321·

CPAP SYSTEM, MODEL 102001

FDA 510(k)

FDA Class 2 ·Anesthesiology

EARGO

FDA UDI

Eargo, Inc.·00850010429137·EARGO NEO HiFi System

SILENT PARTNER MODEL 10-2001

FDA 510(k)

FDA Class 2 ·Anesthesiology

SEKISUI DIAGNOSTICS, LLC

FDA registration

SEKISUI DIAGNOSTICS, LLC·1 product·🇺🇸 United States

Smart Flow Neuro Ventricular Cannula, 14 ga, 21” ID x 10 ft x 15mm tip

FDA registration

Sterigenics U.S., LLC·1 product·🇺🇸 United States

Acucy System; Part Number 1039

FDA registration

HAMAMATSU PHOTONICS ELECTRON TUBE DIVISION·1 product·🇯🇵 Japan

BREEZE SLEEPGEAR WITH DREAMSEAL

FDA 510(k)

FDA Class 2 ·Anesthesiology

SMARTSCREW

FDA 510(k)

FDA Class 2 ·Orthopedic

K1025-01-EDT

Basic UDI-DI

EU MDR · Eu Md Class 2a ·6 devices