SOUNDSTAR 3D G (SNDSTR10G)

FDA registration

THE STANDARD CO., LTD.·1 product·🇰🇷 South Korea

SoundStar 3D 10F Diagnostic Ultrasound Catheter

FDA registration

Siemens Healthineers Ltd.·1 product·🇰🇷 South Korea

BIOSENSE WEBSTER, INC.

FDA registration

BIOSENSE WEBSTER, INC.·1 product·🇺🇸 United States

SOUNDSTAR 3D ULTRASOUND CATHETER, MODEL M-5723-12

FDA registration

LARK INDUSTRIES·1 product·🇺🇸 United States

SOUNDSTAR G 10F-90, GE

FDA registration

GMED Healthcare BVBA ( a Johnson & Johnson Company)·1 product·🇧🇪 Belgium

SOUNDSTAR 3D ULTRASOUND CATHETER, MODEL M-5723-12

FDA 510(k)

FDA Class 2 ·Cardiovascular

Catheter, Ultrasound, Intravascular

FDA classification

FDA Class 2 ·Catheter, Ultrasound, Intravascular

DELTA

FDA UDI

Stryker Leibinger GmbH & Co. KG·07613327373554·S-Drill Tap, Hex 43mm, 2.2 X 4mm Screw

De Soutter Medical

FDA UDI

DE SOUTTER MEDICAL LIMITED·05051471122819·K-WIRE - DOUBLE TROCAR 0.6mm DIA x 100mm

appliance, fixation, nail/blade/plate combination, multiple component Reprocessed External Fixation Devices

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

StrykerSustainability (SDA) - Reprocessed External Fixation Devices

FDA registration

Isomedix Operations Inc.·1 product·🇺🇸 United States

MAINLINE MEDICAL DENTAL SUPPLY

FDA registration

MAINLINE MEDICAL DENTAL SUPPLY·1 product·🇨🇦 Canada

Cardinal Health

FDA registration

Cardinal Health·1 product·🇺🇸 United States

Cardinal Health 200, LLC

FDA registration

Cardinal Health 200, LLC·1 product·🇺🇸 United States

Reprocessed External Fixation Device

FDA registration

Stryker Sustainability Solutions Phoenix·1 product·🇺🇸 United States

Reprocessed External Fixation Device

FDA registration

Stryker Sustainability Solutions·1 product·🇺🇸 United States

Model 220, Patient Magnet

FDA registration

LivaNova USA, Inc.·1 product·🇺🇸 United States

THEKEN CPOD/LPOD VERTEBRAL BODY REPLACEMENT SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

COMFIT CHEMO PLUS POWDER FREE BLUE NITRILE EXAMINATION GLOVES, NON STERILE (TESTED FOR USE WITH CHEMOTHERAPY DRUG) LABEL

FDA 510(k)

FDA Class 1 ·General Hospital

Spinal Vertebral Body Replacement Device

FDA classification

FDA Class 2 ·Spinal Vertebral Body Replacement Device