Intervertebral fusion device with bone graft, lumbar

FDA registration

SOLCO BIOMEDICAL COMPANY INDIA PRIVATE LIMITED·1 product·🇮🇳 India

CEZANNE Lumbar Interbody Fusion Cage System

FDA registration

CTL Medical Corporation·1 product·🇺🇸 United States

ORACLE LUMBAR INTERVERTEBRAL BODY FUSION CAGE SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

StimuCath (19 Ga)

FDA registration

Arrow International, LLC (subsidiary of Teleflex Incorporated)·1 product·🇺🇸 United States

StimuCath (19 Ga)

FDA registration

Arrow International LLC (subsidiary of Teleflex Incorporated)·1 product·🇺🇸 United States

StimuCath (19 Ga)

FDA registration

Teleflex LLC (NADC 2)·1 product·🇺🇸 United States

StimuCath (19 Ga)

FDA registration

Arrow International CR, a.s.·1 product·🇨🇿 Czechia

Arrow Select Kits

FDA registration

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

LNS-17GAL

FDA registration

Ningbo HSCC Medical Technology Co., Ltd·1 product·🇨🇳 China

StimuCath (19 Ga)

FDA registration

Arrow Internacional de Chihuahua S.A. de C.V.·1 product·🇲🇽 Mexico

MEDSOURCE FACTORY,INC.

FDA registration

MEDSOURCE FACTORY,INC.·1 product·🇨🇳 China

STERIS AST CZ s.r.o.

FDA registration

STERIS AST CZ s.r.o.·1 product·🇨🇿 Czechia

Sharp Container

FDA registration

JIANGSU WLD MEDICAL CO., LTD.·1 product·🇨🇳 China

Sharp Container

FDA registration

JCMED TIANJIN IMPORT AND EXPORT CO., LTD·1 product·🇨🇳 China

StimuCath (19 Ga)

FDA registration

Arrow International C.R. a.s.·1 product·🇨🇿 Czechia

Eurotrol Hct Control, Level A - 1950210

FDA registration

EUROTROL B.V.·1 product·🇳🇱 Netherlands

Altis Single Incision Sling System

FDA registration

COLOPLAST MANUFACTURING US, LLC·1 product·🇺🇸 United States

SHARPS CONTAINER

FDA 510(k)

FDA Class 2 ·General Hospital

STIMUCATH CONTINUOUS NERVE BLOCK SET, PRODUCT NUMBER AB-05000

FDA 510(k)

FDA Class 2 ·Anesthesiology

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

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