MICROPORT ORTHOPEDICS INC.

FDA registration

MICROPORT ORTHOPEDICS INC.·1 product·🇺🇸 United States

CERAMIC FEMORAL HEAD-28MM LONG, MODIFICATION

FDA 510(k)

FDA Class 2 ·Orthopedic

Solstice Occipito-Cervico-Thoracic System

FDA UDI

Life Spine, Inc.·00190837014988·

Duo Lumbar Interbody Fusion Device

FDA UDI

SPINEOLOGY INC.·M7402925512·Duo, Hyper-Lordotic, 55 x 12mm

DURACON TOTAL KNEE SYSTEM TIBIAL COMPONENTS

FDA registration

SCT, INC.·1 product·🇺🇸 United States

One way valve, 1950000, 1952000, 1954000

FDA registration

UAB INTERSURGICAL·1 product·🇱🇹 Lithuania

ISOMEDIX OPERATIONS INC.

FDA registration

ISOMEDIX OPERATIONS INC.·1 product·🇺🇸 United States

Duracon Knee System

FDA registration

HOWMEDICA INTERNATIONAL S. DE R.L.,·1 product·🇮🇪 Ireland

ISOMEDIX OPERATIONS INC.

FDA registration

ISOMEDIX OPERATIONS INC.·1 product·🇺🇸 United States

Duracon Knee System

FDA registration

STRYKER IRELAND OSTEONICS·1 product·🇮🇪 Ireland

Stry Mah

FDA registration

Phillips Precision Inc·1 product·🇺🇸 United States

Duracon Knee System

FDA registration

HOWMEDICA OSTEONICS CORP·1 product·🇺🇸 United States

ALMARK TOOL & MANUFACTURING COMPANY, INC.

FDA registration

ALMARK TOOL & MANUFACTURING COMPANY, INC.·1 product·🇺🇸 United States

ANTERIOR NECK CONTOUR COIL

FDA 510(k)

FDA Class 2 ·Radiology

DURACON TOTAL KNEE SYSTEM TIBIAL COMPONENTS

FDA 510(k)

FDA Class 2 ·Orthopedic

Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

FDA classification

FDA Class 2 ·Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

FDA classification

FDA Class 2 ·Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

System, Nuclear Magnetic Resonance Imaging

FDA classification

FDA Class 2 ·System, Nuclear Magnetic Resonance Imaging