VersaVit Core Essentials Packs

FDA registration

MIDWEST STERILIZATION CORP.·1 product·🇺🇸 United States

VERSAVIT

FDA 510(k)

FDA Class 2 ·Ophthalmic

Instrument, Vitreous Aspiration And Cutting, Ac-Powered

FDA classification

FDA Class 2 ·Instrument, Vitreous Aspiration And Cutting, Ac-Powered

LARGE CANNULATED SCREWS

FDA UDI

Smith & Nephew, Inc.·03596010064219·CANNULATED HIP PIN 135MM

ARROW-LOK Hybrid: Dia. 2.5-3.5mm / Length 25mm Angled (ASTM F138)

FDA registration

Sterigenics U.S., LLC·1 product·🇺🇸 United States

Vu cPOD IBF

FDA registration

SEASPINE ORTHOPEDICS CORPORATION·1 product·🇺🇸 United States

ARROW-LOK Hybrid: Dia. 2.5-3.5mm / Length 25mm Angled (ASTM F138)

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

Millstone Medical Outsourcing LLC

FDA registration

Millstone Medical Outsourcing LLC·1 product·🇺🇸 United States

Arrow-Lok

FDA registration

ARROWHEAD DE LLC·1 product·🇺🇸 United States

ARROW-LOK Hybrid: Dia. 2.5-3.5mm / Length 25mm Angled (ASTM F138)

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

Re-Trace Ureteral Access Sheath

FDA registration

Sterigenics SAS·1 product·🇫🇷 France

Airlife Infant Skin Temp Probe

FDA registration

AirLife Finland Oy·1 product·🇫🇮 Finland

Alcohol Swab

FDA registration

CAREFUSION 2200, INC.·1 product·🇺🇸 United States

VU C*POD INTERVERTEBRAL BODY FUSION DEVICE

FDA 510(k)

FDA Class 2 ·Orthopedic

ARROW-LOK DIGITAL SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

Pin, Fixation, Smooth

FDA classification

FDA Class 2 ·Pin, Fixation, Smooth

Intervertebral Fusion Device With Bone Graft, Cervical

FDA classification

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