L5018-0812

FDA registration

L&K BIOMED CO.,LTD.·1 product·🇰🇷 South Korea

AccelFix Lumbar Expandable Cage System

FDA 510(k)

FDA Class 2 ·Orthopedic

KMEDIC

FDA UDI

TELEFLEX INCORPORATED·24026704261493·LISTER BANDAGE SCISSORS 4 1/2"

NuFACE Mini+

FDA registration

Carol Cole Company·1 product·🇺🇸 United States

Streamline Surgical System

FDA registration

New World Medical, Inc.·2 products·🇺🇸 United States

NuFACE Mini Plus

FDA registration

Key Tronic Juarez, S.A de C.V.·1 product·🇲🇽 Mexico

AirLife DuoTherm® Temperature Probe, Reusable, 180 cm

FDA registration

WILAMED GMBH·2 products·🇩🇪 Germany

Celect Platinum® Vena Cava Filter Set for Femoral and Jugular Vein Approach

FDA registration

WILLIAM COOK EUROPE APS·1 product·🇩🇰 Denmark

Cook Medical EUDC GmbH

FDA registration

Cook Medical EUDC GmbH·1 product·🇩🇪 Germany

SPECTRAPULSE

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

NuFACE Mini Plus

FDA 510(k)

FDA Class 2 ·Neurology

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar

Stimulator, Transcutaneous Electrical, Aesthetic Purposes

FDA classification

FDA Class 2 ·Stimulator, Transcutaneous Electrical, Aesthetic Purposes

Powered Laser Surgical Instrument

FDA classification

FDA Class 2 ·Powered Laser Surgical Instrument