Iontophor

FDA registration

WR MEDICAL ELECTRONICS CO.·1 product·🇺🇸 United States

MODIFIED USE FOR MODEL 6110A IONTOPHORETIC APPLI.

FDA 510(k)

FDA Class 2 ·Physical Medicine

Device, Iontophoresis, Other Uses

FDA classification

FDA Class 2 ·Device, Iontophoresis, Other Uses

Flex-IT

FDA registration

EVERLIFE MEDICAL EQUIPMENT CO., LTD.·2 products·🇹🇼 Taiwan

Sutter CURIS RF Generator

FDA registration

Arthrex Distribution Hub EMEA B.V.·1 product·🇳🇱 Netherlands

SUTTER MEDIZINTECHNIK GMBH

FDA registration

SUTTER MEDIZINTECHNIK GMBH·1 product·🇩🇪 Germany

Sutter CURIS RF Generator

FDA registration

Arthrex GmbH·1 product·🇩🇪 Germany

Flex-IT

FDA registration

EMSI·2 products·🇺🇸 United States

Sutter CURIS RF Generator

FDA registration

Arthrex Singapore Pte Ltd.·1 product·🇸🇬 Singapore

Sutter CURIS RF Generator

FDA registration

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

KLS Martin SE & Co. KG

FDA registration

KLS Martin SE & Co. KG·1 product·🇩🇪 Germany

Venti-Scan IV

FDA registration

MIRION TECHNOLOGIES (CAPINTEC), INC·1 product·🇺🇸 United States

TENS/IF 14

FDA 510(k)

FDA Class 2 ·Neurology

Sutter CURIS RF Generator

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Stimulator, Nerve, Transcutaneous, For Pain Relief

FDA classification

FDA Class 2 ·Stimulator, Nerve, Transcutaneous, For Pain Relief

Electrosurgical, Cutting & Coagulation & Accessories

FDA classification

FDA Class 2 ·Electrosurgical, Cutting & Coagulation & Accessories