SPINE WAVE, INC.

FDA registration

SPINE WAVE, INC.·2 products·🇺🇸 United States

STAXX(R) SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

Oticon

FDA UDI

Oticon A/S·05707131260529·RIA PRO, RITE 312 WL TC

OVF / Assay, direct, nucleic acid amplification, q fever

FDA registration

MONOCENT INC.·1 product·🇺🇸 United States

TuohySono

FDA registration

PAJUNK GMBH MEDIZINTECHNOLOGIE·1 product·🇩🇪 Germany

TALOS® IBF

FDA UDI

MEDITECH SPINE, LLC·B1671332070·

Gel-Bead embolizaion spheres

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

CIRRUS Photo Models 600 and 800

FDA registration

CARL ZEISS MEDITEC AG (JENA)·2 products·🇩🇪 Germany

Spinal Vertebral Body Replacement Device

FDA classification

FDA Class 2 ·Spinal Vertebral Body Replacement Device

SONO TAP, TUOHY SONO

FDA 510(k)

FDA Class 2 ·Anesthesiology

JBAIDS Q FEVER DETECTION KIT

FDA 510(k)

FDA Class 1 ·Microbiology

Assay, Direct, Nucleic Acid Amplification, Q Fever

FDA classification

FDA Class 1 ·Assay, Direct, Nucleic Acid Amplification, Q Fever

Needle, Conduction, Anesthetic (W/Wo Introducer)

FDA classification

FDA Class 2 ·Needle, Conduction, Anesthetic (W/Wo Introducer)