IdentiTi

FDA UDI

ALPHATEC SPINE, INC.·00190376174358·TAMP, STRAIGHT

LenSx Laser System

FDA registration

Sterigenics US LLC·3 products·🇺🇸 United States

SYNTHES XRL

FDA 510(k)

FDA Class 2 ·Orthopedic

AGILTRAC .035 PERIPHERAL DILATATION CATHETER

FDA 510(k)

FDA Class 2 ·Cardiovascular

KONG-TL VBR, End Plate, rectangular, M and Screw, 12° x 33 mm

FDA UDI

icotec AG·07640164847702·KONG-TL VBR, End Plate, rectangular, M and Scre...

TWISTOFF® SCREW

FDA UDI

Biomet Orthopedics, LLC·00887868011214·

TWISTOFF® SCREW

FDA UDI

Biomet Orthopedics, LLC·00887868011207·

TALOS® IBF

FDA UDI

MEDITECH SPINE, LLC·B167310123320060·

TWISTOFF® SCREW

FDA UDI

Biomet Orthopedics, LLC·00887868011191·

TWISTOFF® SCREW

FDA UDI

Biomet Orthopedics, LLC·00887868011238·

TALOS® IBF

FDA UDI

MEDITECH SPINE, LLC·B167310123320160·

TWISTOFF® SCREW

FDA UDI

Biomet Orthopedics, LLC·00887868011221·

TALOS® IBF

FDA UDI

MEDITECH SPINE, LLC·B167310123320120·

TALOS® IBF

FDA UDI

MEDITECH SPINE, LLC·B167310123320200·

TALOS® IBF

FDA UDI

MEDITECH SPINE, LLC·B167310123320300·

NEUFLEX

FDA UDI

DEPUY ORTHOPAEDICS, INC.·10603295017905·NEUFLEX FINGER-PIP IMPLANT 2 CEMENTLESS

TALOS® IBF

FDA UDI

MEDITECH SPINE, LLC·B167310123320250·

Spinal Vertebral Body Replacement Device

FDA classification

FDA Class 2 ·Spinal Vertebral Body Replacement Device

Catheter, Percutaneous

FDA classification

FDA Class 2 ·Catheter, Percutaneous