Contego Medical, Inc.

7 product lines across 4 device categories: Angioplasty balloons, Carotid stents, Embolic protection, Thrombectomy devices.

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Peripheral Angioplasty Balloons

Used in: DVT Mechanical Thrombectomy, Venous Stenting (Iliac and Central Veins), Peripheral Balloon Angioplasty, Peripheral Artery Stenting, Peripheral Atherectomy, Fistulogram with Angioplasty

ProductSizes (FDA GUDID)ModelsMRI
Paladin
The Paladin Carotid PTA Balloon System with Integrated Embolic Protection (IEP), is indicated for Percutaneous Transluminal Angioplasty (PTA) in the carotid arteries…
—4Not stated

Carotid Stents

Used in: Carotid Artery Stenting

ProductSizes (FDA GUDID)ModelsMRI
Neuroguard IEP System
The Neuroguard IEP System consists of three main components: • A self-expanding nitinol stent • A delivery catheter which includes a post-dilation…
—8MR Conditional

Embolic Protection Devices

Used in: Carotid Artery Stenting

ProductSizes (FDA GUDID)ModelsMRI
Vanguard
The Vanguard IEP Peripheral Balloon Angioplasty System with Integrated Embolic Protection is indicated for percutaneous transluminal angioplasty (PTA) and capture and removal…
—6Not stated
Paladin
The Paladin Carotid PTA Balloon System with Integrated Embolic Protection (IEP), is indicated for Percutaneous Transluminal Angioplasty (PTA) in the carotid arteries…
—4Not stated

Mechanical Thrombectomy Devices

Used in: DVT Mechanical Thrombectomy, Pulmonary Embolism Thrombectomy, Dialysis Graft and Fistula Thrombectomy

ProductSizes (FDA GUDID)ModelsMRI
Excipio LV
The Excipio LV Thrombectomy Device is indicated for the non-surgical removal of emboli and thrombi from peripheral blood vessels.
—1Not stated
Excipio SV
The Excipio SV Thrombectomy Device is indicated for the non-surgical removal of soft emboli and thrombi from peripheral blood vessels.
—1Not stated
Excipio LV PRIME Thrombectomy Device
The Excipio® LV PRIME (Large Vessel) Thrombectomy Device (the “Device”) is a rapid exchange (RX) catheter with an integrated nitinol braided basket…
—1Not stated

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Product lines, models and sizes are compiled from the FDA Global Unique Device Identification Database (GUDID) and FDA clearance records. Descriptions marked "Provided by the manufacturer" come from the company and are reviewed before publishing.

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