OneTouch Verio Blood Glucose Monitoring System

FDA registration

LIFESCAN EUROPE GMBH·2 products·🇨🇭 Switzerland

One Touch Verio: Blood Glucose Monitoring System

FDA registration

Flextronics Industrial (Shenzhen) Co., Ltd.·2 products·🇨🇳 China

OneTouch Verio Meter

FDA registration

LIFESCAN SCOTLAND LTD·2 products·🇬🇧 United Kingdom

ONETOUCH VERIO BLOOD GLUCOSE MONITORING SYSTEM

FDA 510(k)

FDA Class 2 ·Clinical Chemistry

Millstone Medical Outsourcing LLC

FDA registration

Millstone Medical Outsourcing LLC·1 product·🇺🇸 United States

STRUCTURE MEDICAL, LLC.

FDA registration

STRUCTURE MEDICAL, LLC.·1 product·🇺🇸 United States

Vu cPOD IBF

FDA registration

SEASPINE ORTHOPEDICS CORPORATION·1 product·🇺🇸 United States

Structure Medical, LLC.

FDA registration

Structure Medical, LLC.·1 product·🇺🇸 United States

PPX urine, EasyRA assay

FDA registration

MEDICA CORP.·3 products·🇺🇸 United States

Convertors de Mexico S. de R.L. de C.V

FDA registration

Convertors de Mexico S. de R.L. de C.V·1 product·🇲🇽 Mexico

Synergy Health Marseille SAS

FDA registration

Synergy Health Marseille SAS·1 product·🇫🇷 France

HR PHARMACEUTICALS, INC d/b/a HR HealthCare

FDA registration

HR PHARMACEUTICALS, INC d/b/a HR HealthCare·1 product·🇺🇸 United States

DOLPHIX EXTERNAL FIXATION SYSTEM

FDA registration

ARTHREX, INC.·2 products·🇺🇸 United States

Sterigenics US LLC

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

VU CPOD INTERVERTEBRAL BODU FUSION DEVICE

FDA 510(k)

FDA Class 2 ·Orthopedic

QCA (VERSION 3.1)

FDA 510(k)

FDA Class 2 ·Hematology

System, Test, Blood Glucose, Over The Counter

FDA classification

FDA Class 2 ·System, Test, Blood Glucose, Over The Counter

Microscope, Automated, Image Analysis, Immunohistochemistry,Operator Intervention,Nuclear Intensity & Percent Positivity

FDA classification

FDA Class 2 ·Microscope, Automated, Image Analysis, Immunohistochemistry,Operator Intervention,Nuclear Intensity & Percent Positivity

Intervertebral Fusion Device With Bone Graft, Cervical

FDA classification

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