Trial - Foundation 3D Plif - 30mm X 10mm X 14mm, 7° 02P01351

FDA registration

STRAITS ORTHOPAEDICS (MFG) SDN BHD·2 products·🇲🇾 Malaysia

Trial - Foundation 3D Plif - 30mm X 10mm X 14mm, 7° 02P01351

FDA registration

STRAITS ORTHOPAEDICS (MFG) SDN BHD·2 products·🇲🇾 Malaysia

Sterigenics US LLC

FDA registration

Sterigenics US LLC·2 products·🇺🇸 United States

FOUNDATION 3D INTERBODY SYSTEM

FDA registration

SURGICAL INSTRUMENT MANUFACTURERS, LLC·2 products·🇺🇸 United States

INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, LUMBAR

FDA registration

ZAVATION·2 products·🇺🇸 United States

Trial - Foundation 3D Plif - 30mm X 10mm X 14mm, 7° 02P01351

FDA registration

STRAITS ORTHOPAEDICS (MFG) SDN BHD·2 products·🇲🇾 Malaysia

Trial - Foundation 3D Plif - 30mm X 10mm X 14mm, 7° 02P01351

FDA registration

STRAITS ORTHOPAEDICS (MFG) SDN BHD·2 products·🇲🇾 Malaysia

Isomedix Operations, Inc.

FDA registration

Isomedix Operations, Inc.·2 products·🇺🇸 United States

Trial - Foundation 3D Plif - 30mm X 10mm X 14mm, 7° 02P01351

FDA registration

Straits Orthopaedics (MFG) Sdn Bhd·2 products·🇲🇾 Malaysia

Foundation 3D Interbody

FDA 510(k)

FDA Class 2 ·Orthopedic

OSTEOPORE TCP

FDA registration

SPINECRAFT LLC·1 product·🇺🇸 United States

Millstone Medical Outsourcing LLC

FDA registration

Millstone Medical Outsourcing LLC·3 products·🇺🇸 United States

Cross-Fuse II PEEK IBF System

FDA registration

Xtant Medical Holdings, Inc.·3 products·🇺🇸 United States

LuminScanTM Imaging System Console-EOCT-C1-10-10-Disposable Imaging Kit-BOP-20-30-25-7

FDA registration

Micro-Tech (Nanjing) Co., Ltd.·1 product·🇨🇳 China

Supercath5

FDA registration

TOGO MEDIKIT CO., LTD.·1 product·🇯🇵 Japan

Arthrosurface® Total Toe - Proximal Phalanx Implant

FDA registration

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

LuminScanTM Imaging System Console-EOCT-C1-10-10-Disposable Imaging Kit-BOP-20-30-25-7

FDA registration

Micro-Tech (Nanjing) Co., Ltd.·1 product·🇨🇳 China

OSTEOPORE TCP

FDA 510(k)

FDA Class 2 ·Orthopedic

POWERHEART AED G3 SEMI-AUTOMATIC, POWERHEART AED G3 AUTOMATIC, POWERHEART AED G3 PRO, POWERHEART AED G3 PLUS

FDA 510(k)

FDA Class 3 ·Cardiovascular

Intervertebral Fusion Device With Bone Graft, Cervical

FDA classification

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