AEVUMED PHANTOM SUTURE ANCHORS

FDA registration

NextPhase Medical Devices LLC·1 product·🇺🇸 United States

AEVUMED PHANTOM Suture Anchors

FDA 510(k)

FDA Class 2 ·Orthopedic

Maestro™ Total Wrist

FDA UDI

Biomet Orthopedics, LLC·00887868240102·

MAESTRO TOTAL WRIST

FDA UDI

Biomet Orthopedics, LLC·00880304555266·

INNESIS PEEK CAGE

FDA registration

BK MEDITECH, USA·1 product·🇺🇸 United States

uTASWako AFP-L3 Control L and H

FDA registration

FUJIFILM Wako Pure Chemical Corporation Diagnostics Design Office (Amagasaki)·5 products·🇯🇵 Japan

uTASWako AFP-L3 Control L and H

FDA registration

FUJIFILM Healthcare Manufacturing Corporation MIE Office·5 products·🇯🇵 Japan

INNESIS PEEK CAGE

FDA registration

BK MEDITECH CO., LTD.·1 product·🇰🇷 South Korea

FUJIFILM Healthcare Americas Corporation

FDA registration

FUJIFILM Healthcare Americas Corporation·5 products·🇺🇸 United States

FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Takematsu Office

FDA registration

FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Takematsu Office·5 products·🇯🇵 Japan

Gold Standard Diagnostics Borrelia Burgdorferi Igg/Igm ELISA Test Kit

FDA registration

Gold Standard Diagnostics Frankfurt GmbH·1 product·🇩🇪 Germany

INNESIS PEEK CAGE

FDA 510(k)

FDA Class 2 ·Orthopedic

UTASWAKO I30 (INCLUDES ACCESSORIES), UTASWAKO AFP-L3, CALIBRATOR SET, CONTROL L, CONTROL H, SAMPLE DILUTION

FDA 510(k)

FDA Class 2 ·Immunology

Fastener, Fixation, Nondegradable, Soft Tissue

FDA classification

FDA Class 2 ·Fastener, Fixation, Nondegradable, Soft Tissue

Test, Alpha Fetoprotein L3 Subfraction (Afp-L3%), For Hepatocellular Carcinoma Risk Assessment

FDA classification

FDA Class 2 ·Test, Alpha Fetoprotein L3 Subfraction (Afp-L3%), For Hepatocellular Carcinoma Risk Assessment

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

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