CARDIOBLATE GEMINI

FDA registration

CEA Medical Manufacturing, Inc. d.b.a Nissha Medical Technologies·1 product·🇺🇸 United States

CARDIOBLATE GEMINI

FDA registration

MEDTRONIC PERFUSION SYSTEMS·1 product·🇺🇸 United States

CARDIOBLATE GEMINI SURGICAL ABLATION DEVICE

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Surgical Device, For Cutting, Coagulation, And/Or Ablation Of Tissue, Including Cardiac Tissue

FDA classification

FDA Class 2 ·Surgical Device, For Cutting, Coagulation, And/Or Ablation Of Tissue, Including Cardiac Tissue

ASSUFIL

FDA registration

Assut Europe S.P.A.·1 product·🇮🇹 Italy

H200 Wireless

FDA registration

Bioventus LLC·1 product·🇺🇸 United States

H200 Wireless System

FDA registration

BIONESS MEDICAL, INC.·1 product·🇺🇸 United States

Eurotrol Hct Control, Level A - 1950210

FDA registration

EUROTROL B.V.·1 product·🇳🇱 Netherlands

CoSense CO Monitor

FDA registration

CAPNIA, INC.·1 product·🇺🇸 United States

Sterigenics US LLC

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

ASSUFIL

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

NESS H200 WIRELESS HAND REHABILITATION SYSTEM USER KIT AND CLINICAN KIT

FDA 510(k)

FDA Class 2 ·Neurology

Stimulator, Neuromuscular, External Functional

FDA classification

FDA Class 2 ·Stimulator, Neuromuscular, External Functional

Suture, Absorbable, Synthetic, Polyglycolic Acid

FDA classification

FDA Class 2 ·Suture, Absorbable, Synthetic, Polyglycolic Acid