Kardioscreen

FDA registration

IMEDRIX DIAGNOSTICS CORPORATION·1 product·🇺🇸 United States

KardioScreen

FDA 510(k)

FDA Class 2 ·Cardiovascular

CMS8000 Patient Monitor

FDA registration

CONTEC MEDICAL SYSTEMS CO., LTD·10 products·🇨🇳 China

AESCULAP, INC.

FDA registration

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

Craniofix Peek

FDA registration

AESCULAP AG·1 product·🇩🇪 Germany

Biodesign Plastic Surgery Matrix

FDA registration

COOK BIOTECH, INC.·3 products·🇺🇸 United States

NuFACE Mini Facial and Neck Skin Toning Device

FDA registration

Carol Cole Company·1 product·🇺🇸 United States

Biodesign Tissue Graft

FDA registration

COOK INCORPORATED·3 products·🇺🇸 United States

TheraGenesis Non-Meshed Bilayer Wound Matrix

FDA registration

GUNZE LIMITED·1 product·🇯🇵 Japan

AESCULAP PEEK CRANIOFIX

FDA 510(k)

FDA Class 2 ·Neurology

PATIENT MONITOR

FDA 510(k)

FDA Class 2 ·Cardiovascular

Electrocardiograph

FDA classification

FDA Class 2 ·Electrocardiograph

Cover, Burr Hole

FDA classification

FDA Class 2 ·Cover, Burr Hole

Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

FDA classification

FDA Class 2 ·Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)