OWL GD-PAD PATIENT RETURN ELECTRODE

FDA registration

DIROS TECHNOLOGY, INC.·1 product·🇨🇦 Canada

DYNAMIC DIAGNOSTICS INCORPORATED

FDA registration

DYNAMIC DIAGNOSTICS INCORPORATED·1 product·🇺🇸 United States

PROPLATE

FDA registration

BIO PROTECH YANTAI INC·1 product·🇨🇳 China

PROPLATE

FDA registration

BIO PROTECH, INC.·1 product·🇰🇷 South Korea

PROPLATE

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Leforte System Bone Plate

FDA registration

JEIL MEDICAL CORPORATION·1 product·🇰🇷 South Korea

RANDOX LITHIUM

FDA registration

RANDOX LABORATORIES LIMITED·1 product·🇬🇧 United Kingdom

HemosIL Fibrinogen-C

FDA registration

INSTRUMENTATION LABORATORY CO.·1 product·🇺🇸 United States

HemosIL Fibrinogen-C

FDA registration

Instrumentation Laboratory Co.·1 product·🇺🇸 United States

LEFORTE SYSTEM BONE PLATE

FDA 510(k)

FDA Class 2 ·Orthopedic

DFINER UROLOGICAL CATHETER

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

Catheter, Urethrographic, Male

FDA classification

FDA Class 2 ·Catheter, Urethrographic, Male

Appliance, Fixation, Nail/Blade/Plate Combination, Single Component

FDA classification

FDA Class 2 ·Appliance, Fixation, Nail/Blade/Plate Combination, Single Component

Electrosurgical, Cutting & Coagulation & Accessories

FDA classification

FDA Class 2 ·Electrosurgical, Cutting & Coagulation & Accessories