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Contego Medical, Inc.

Last updated September 17, 2026

Information

Country: US
Address: 3801 Lake Boone Trail, Suite 100, Raleigh, NC, 27607
Website: contegomedical.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: +1-919-459-7250
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 3011471056
DUNS Number: 048268128

Catalogue (29)

Device	Model / Reference	Registries	Class	Status
Vanguard	6200x135	FDA UDI	Class II	Active
Neuroguard IEP® System	NG-NV-6-30	FDA UDI	Class III	Active
Vanguard	6120x135	FDA UDI	Class II	Active
Paladin	5.5.x20	FDA UDI	Class II	Active
Paladin	5.5x30	FDA UDI	Class II	Active
Vanguard	5080x135	FDA UDI	Class II	Active
Neuroguard IEP® System	NG-0630-140-2	FDA UDI	Class III	Active
Paladin	5x20	FDA UDI	Class II	Active
Vanguard	5200x135	FDA UDI	Class II	Active
Neuroguard IEP® System	NG-0640-140-2	FDA UDI	Class III	Active
Excipio® LV PRIME Thrombectomy Device	EXC-1607-150	FDA UDI	Class II	Active
Neuroguard IEP® System	NG-NV-6-40	FDA UDI	Class III	Active
Neuroguard IEP® System	NG-0740-140-2	FDA UDI	Class III	Active
Paladin	5x30	FDA UDI	Class II	Active
Neuroguard IEP® System	NG-NV-7-30	FDA UDI	Class III	Active
Vanguard	6080x135	FDA UDI	Class II	Active
Excipio SV	EXC-0940-165	FDA UDI	Class II	Active
Neuroguard IEP® System	NG-0730-140-2	FDA UDI	Class III	Active
Excipio LV	EXC-2510-125	FDA UDI	Class II	Active
Neuroguard IEP® System	NG-NV-7-40	FDA UDI	Class III	Active
Vanguard	5120x135	FDA UDI	Class II	Active
Paladin Carotid Post-Dilation Balloon System with Integrated Embolic Protection	K221339	FDA 510(k)	Class II	Active
Paladin Carotid Post-dilation Balloon System with Integrated Embolic Protection (Paladin System)	K181128	FDA 510(k)	Class II	Active
Excipio LV Thrombectomy Device	K223897	FDA 510(k)	Class II	Active
Vanguard IEP Peripheral Balloon Angioplasty System with Integrated Embolic Protection	K181529	FDA 510(k)	Class II	Active
Excipio SV Aspiration Catheter and Tubing	K230030	FDA 510(k)	Class II	Active
Excipio SV Thrombectomy Device	K221204	FDA 510(k)	Class II	Active
Excipio LV Prime Thrombectomy Device	K251485	FDA 510(k)	Class II	Active
Neuroguard IEP® 3-in-1 Carotid Stent and Post-Dilation Balloon System with Integrated Embolic Protection – (Neuroguard I	P240009	FDA PMA	Class III	Active

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FDA Recalls (1)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
Sep 4, 2025	Z-0131-2026	—	open, classified	Carotid stent and post-dilation balloon system with integrated embolic protection system has an integrated filter that may not open or may not fully open during sheath retraction and operation of the filter knob. The stent is used with a primary distal embolic protection device.