CONCORDE BULLET Lumbar Interbody System

FDA registration

MEDOS INTERNATIONAL SARL·2 products·🇨🇭 Switzerland

Concorde Bullet

FDA registration

Jabil Switzerland Manufacturing GmbH (Le Locle)·2 products·🇨🇭 Switzerland

Concorde Bullet

FDA registration

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

Jabil8683 (DK) - Concorde Bullet Spinal System

FDA registration

Synergy Health Daniken AG·2 products·🇨🇭 Switzerland

CONCORDE Bullet Lumbar Interbody System

FDA registration

EXEL INC. DBA DHL SUPPLY CHAIN (USA)·2 products·🇺🇸 United States

CONCORDE Bullet Lumbar Interbody System

FDA 510(k)

FDA Class 2 ·Orthopedic

Ophthalmic Speculum

FDA UDI

KATENA PRODUCTS, INC.·00841668100226·THORLAKSON ASPIRATING SPECULUM

Model 3873 1 X 8 Lead

FDA registration

MEDTRONIC PUERTO RICO OPERATIONS CO., VILLALBA·1 product·🇺🇸 United States

Model 3873 1 X 8 Lead

FDA registration

Medtronic Engineering and Innovation Center (MEIC)·1 product·🇮🇳 India

Model 3873 1 X 8 Lead

FDA registration

MEDTRONIC NEUROMODULATION·1 product·🇺🇸 United States

Nellcor OxiMax

FDA registration

RENU MEDICAL, INC.·1 product·🇺🇸 United States

CAPSO VIEW SOFTWARE (CAPSO2758)

FDA registration

PENTAX of America, Inc.·1 product·🇺🇸 United States

iCT

FDA registration

Grand Medical Equipment, Inc.·1 product·🇺🇸 United States

Mespere VENUS 2000

FDA registration

MESPERE LIFESCIENCES INC.·1 product·🇨🇦 Canada

MODEL 3873 1* 8 AND MODEL 3874 1* 8 COMPACT TEST STIMULATION LEADS

FDA 510(k)

FDA Class 2 ·Neurology

RENU MEDICAL REPROCESSED OXIMAX SENSORS: ADULT, PEDIATRIC, INFANT AND NEONATE

FDA 510(k)

FDA Class 2 ·Cardiovascular

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

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

Oximeter, Reprocessed

FDA classification

FDA Class 2 ·Oximeter, Reprocessed

Stimulator, Spinal-Cord, Implanted (Pain Relief)

FDA classification

FDA Class 2 ·Stimulator, Spinal-Cord, Implanted (Pain Relief)