Explorer TO System

FDA registration

SEASPINE ORTHOPEDICS CORPORATION·1 product·🇺🇸 United States

Explorer TO System

FDA 510(k)

FDA Class 2 ·Orthopedic

Bernafon

FDA UDI

Bernafon AG·05711584114414·CO9 B 105, 2.4G NFM SABE/MAC CAPTO 9 GPL

Phadia 250 and Phadia 2500, Phadia 5000 Instrument E series

FDA registration

PHADIA GMBH·1 product·🇩🇪 Germany

S-Mini Implant System

FDA registration

NEOBIOTECH CO., LTD.·1 product·🇰🇷 South Korea

Phadia 250 and Phadia 2500, Phadia 5000 Instrument E series

FDA registration

PHADIA AB·1 product·🇸🇪 Sweden

Phadia 250 and Phadia 2500, Phadia 5000 Instrument E series

FDA registration

PHADIA AB·1 product·🇸🇪 Sweden

Phadia 250 and Phadia 2500, Phadia 5000 Instrument E series

FDA registration

PHADIA US INC.·1 product·🇺🇸 United States

Unity

FDA UDI

DIOMEDICAL CO.,LTD.·08800039821643·SIJ Lag ScrewOD12.5xL40

EXPERIENCE®

FDA UDI

Gc Orthodontics America Inc.·D78821254000201·EXPERIENCE Mini MBT 022/U4 UNIV-7T 0A

Lianyungang Anson Non-woven Product Co., Ltd.

FDA registration

Lianyungang Anson Non-woven Product Co., Ltd.·1 product·🇨🇳 China

Catheter, Percutaneous, Neurovasculature

FDA registration

NEURAVI LIMITED·1 product·🇮🇪 Ireland

CAM A P I MEDICAL CO., LTD.

FDA registration

CAM A P I MEDICAL CO., LTD.·1 product·🇰🇭 Cambodia

BLY-501 ADAPTOR

FDA 510(k)

FDA Class 2 ·Cardiovascular

S-MINI IMPLANT SYSTEM

FDA 510(k)

FDA Class 2 ·Dental

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

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

Electrocardiograph

FDA classification

FDA Class 2 ·Electrocardiograph

Implant, Endosseous, Root-Form

FDA classification

FDA Class 2 ·Implant, Endosseous, Root-Form