MICROPORT ORTHOPEDICS INC.

FDA registration

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

LACEY REVISION FEMORAL COMPONENT

FDA 510(k)

FDA Class 2 ·Orthopedic

Lode B.V.

FDA UDI

Lode B.V.·08717524640194·925900 Excalibur Sport

Lode B.V.

FDA UDI

Lode B.V.·08717524641054·965910 Excalibur Sport

Medline

FDA UDI

MEDLINE INDUSTRIES, INC.·10888277396999·K9-2590-50 TAVA SURGICAL SAGITTAL/OSC S

Medline

FDA UDI

MEDLINE INDUSTRIES, INC.·10888277392991·K9-2590-50 SAGITTAL/OSC SB,LG BONE FOR

ZEST ANCHORS, LLC

FDA registration

ZEST ANCHORS, LLC·1 product·🇺🇸 United States

Berichrom Heparin

FDA registration

Siemens Healthcare Diagnostics Products GmbH·1 product·🇩🇪 Germany

ZEST ANCHORS, LLC

FDA registration

ZEST ANCHORS, LLC·1 product·🇺🇸 United States

INFRARED LAMP

FDA 510(k)

FDA Class 2 ·Physical Medicine

POLAMEDCO TRACHEAL AND NASOTRACHEAL TUBES

FDA 510(k)

FDA Class 2 ·Anesthesiology

NA

FDA UDI

STERILMED, INC.·10888551007559·SAW BLADE SAGITTAL K9 K2000 SERIES

NA

FDA UDI

STERILMED, INC.·10888551007597·SAW BLADE SAGITTAL K9 K2000 SERIES

NA

FDA UDI

STERILMED, INC.·10888551007603·SAW BLADE SAGITTAL K9 K2000 SERIES

NA

FDA UDI

STERILMED, INC.·10888551007566·SAW BLADE SAGITTAL K9 K2000 SERIES

NA

FDA UDI

STERILMED, INC.·10888551007573·SAW BLADE SAGITTAL FLARED K9 K2000 SERIES

NA

FDA UDI

STERILMED, INC.·10888551007580·SAW BLADE SAGITTAL K9 K2000 SERIES

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

FDA classification

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

Lamp, Infrared, Therapeutic Heating

FDA classification

FDA Class 2 ·Lamp, Infrared, Therapeutic Heating

Tube, Tracheal (W/Wo Connector)

FDA classification

FDA Class 2 ·Tube, Tracheal (W/Wo Connector)