Genii Active Cord (G1112006) (EN-CFE)

FDA registration

UNITED STATES ENDOSCOPY GROUP, INC.·1 product·🇺🇸 United States

Genii

FDA registration

CINTRON MEDICAL CORPORATION·1 product·🇺🇸 United States

GENII GI 4000 ELECTROSUGICAL GENERATOR

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

TruArch Cannulated Subtalar Implant System

FDA registration

Ascension Orthopedics, Inc.·1 product·🇺🇸 United States

VALIDATE Chem 7 Calibration Verification Test Set

FDA registration

LGC Clinical Diagnostics, Inc.·1 product·🇺🇸 United States

CapSure® Spine System

FDA UDI

Spine Wave, Inc.·10840642104448·Rod Straight 5.5 x 65mm

Puregraft 850 system

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

Artisyn Y-Shaped Mesh

FDA registration

Johnson & Johnson MEDICAL GmbH·1 product·🇩🇪 Germany

Gauge, Pressure, Coronary, Cardiopulmonary Bypass

FDA registration

MEDTRONIC PERFUSION SYSTEMS·1 product·🇺🇸 United States

Gauge, Pressure, Coronary, Cardiopulmonary Bypass

FDA registration

Medtronic Grand Rapids·1 product·🇺🇸 United States

VALIDATE CHEM 7 CALIBRATION VERIFICATION TEST SET, MODEL 10007

FDA 510(k)

FDA Class 1 ·Clinical Chemistry

NHANES WHOLE BODY DXA REFERENCE DATABASE

FDA 510(k)

FDA Class 2 ·Radiology

Electrosurgical, Cutting & Coagulation & Accessories

FDA classification

FDA Class 2 ·Electrosurgical, Cutting & Coagulation & Accessories

Densitometer, Bone

FDA classification

FDA Class 2 ·Densitometer, Bone

Multi-Analyte Controls, All Kinds (Assayed)

FDA classification

FDA Class 1 ·Multi-Analyte Controls, All Kinds (Assayed)