TRUIS Lumbar Intervertebral Body Fusion Cage System

FDA registration

L&K BIOMED CO.,LTD.·1 product·🇰🇷 South Korea

VENUS LUMBAR INTERVERTEBRAL BODY FUSION CAGE SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

HT III SA FIXTURE SYSTEM

FDA registration

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

Models 1804, 1805, 1806, 1807, 2302, 2303, 2304, 2305, 2306, ARCS

FDA registration

Biox Instruments Co Ltd·2 products·🇨🇳 China

HT III SA FIXTURE SYSTEM

FDA registration

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

Merit Medical®

FDA UDI

Merit Medical Systems, Inc.·00884450459850·

21-Hydroxylase Autoantibody ELISA, EIA-5955

FDA registration

DRG International, Inc.·1 product·🇺🇸 United States

(1M2006; 1M2009; 1M2012) FlowEase Subcutaneous Infusion Set

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

EnSite Array Catheter

FDA registration

MIDWEST STERILIZATION CORP.·1 product·🇺🇸 United States

21-Hydroxylase Autoantibody ELISA, EIA-5955

FDA registration

DRG INSTRUMENTS GMBH·1 product·🇩🇪 Germany

HT III SA FIXTURE SYSTEM

FDA 510(k)

FDA Class 2 ·Dental

X-SIZER CATHETER SYSTEM

FDA 510(k)

FDA Class 2 ·Cardiovascular

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

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

Catheter, Peripheral, Atherectomy

FDA classification

FDA Class 2 ·Catheter, Peripheral, Atherectomy

Implant, Endosseous, Root-Form

FDA classification

FDA Class 2 ·Implant, Endosseous, Root-Form