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SPINEOLOGY INC.

Last updated September 17, 2026

Information

Country: US
Address: 7800 THIRD STREET N., Saint Paul, MN, 55128
Website: spineology.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: 651-256-8500
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 3003179719
DUNS Number: 033014361

Catalogue (1995)

Page 2 of 40

Device	Model / Reference	Registries	Class	Status
Fortress Rod	10-10-51-5	FDA UDI	Class II	Active
Discectomy Set	10-01-136	FDA UDI	Class I	Active
CAPTURE Facet Screw Set System	70-02-038	FDA UDI	Class I	Active
Threshold Pedicular Fixation System	53-07-13	FDA UDI	Class I	Active
Threshold V2 Pedicle Screw	10-10-78-39	FDA UDI	Class II	Active
Fortress Pedicale Screw	10-10-57-2	FDA UDI	Class II	Unknown
Elite Expandable Interbody Fusion System	10-01-23	FDA UDI	Class I	Active
Threshold Pedicular Fixation System	55-02-01-075	FDA UDI	Class I	Active
Merlon Retractor System	19-01-09-06	FDA UDI	Class I	Active
SOAR Retractor System	66-03-11	FDA UDI	Class I	Active
Threshold Pedicular Fixation System	10-10-56-5	FDA UDI	Class II	Active
OptiMesh Multiplanar Expandable Interbody Fusion System	35-06-38	FDA UDI	Class I	Active
SOAR Retractor System	78-02-45-5	FDA UDI	Class I	Active
VIA Spinous Process Fixation System	34-12-12	FDA UDI	Class II	Active
Rampart-O	83-05-01-13	FDA UDI	Class I	Active
Navigation	16-02-04	FDA UDI	Class II	Active
Fortress Pedicale Screw	10-10-57-24	FDA UDI	Class II	Unknown
Rampart T Lumbar Interbody Fusion Device	10-10-72-20	FDA UDI	Class II	Unknown
OptiMesh Multiplanar Expandable Interbody Fusion System	32-30-16	FDA UDI	Class I	Active
Fortress Pedicle Screw	10-10-48-20	FDA UDI	Class II	Active
Rampart One Lumbar Interbody Fusion System	49-28-01	FDA UDI	Class II	Active
Rampart O	83-04-07-41	FDA UDI	Class II	Active
SOAR Retractor System	78-02-02-2	FDA UDI	Class I	Active
Capture	70-01-001-5	FDA UDI	Class II	Active
Rampart-T	83-01-05-15	FDA UDI	Class II	Active
Rampart One Lumbar Interbody Fusion Device	10-10-76-5	FDA UDI	Class II	Active
Fortress Rod	10-10-50-11	FDA UDI	Class II	Active
Threshold Pedicular Fixation System	10-62-14	FDA UDI	Class I	Active
SOAR Retractor System	78-02-38-4	FDA UDI	Class I	Active
VIA Spinous Process Fixation System	34-12-10	FDA UDI	Class II	Active
Rampart One Lumbar Interbody Fusion System	49-22-01-3	FDA UDI	Class II	Active
Threshold V2 Pedicular Fixation System	10-10-84-5	FDA UDI	Class II	Active
VIA Spinous Process Fixation System	34-01-06, 07	FDA UDI	Class II	Active
Palisade Pedicular Fixation System	10-10-59-17	FDA UDI	Class II	Active
Duo Lumbar Interbody Fusion Device	10-10-05-38	FDA UDI	Class II	Active
Duo Ti Expandable Interbody Fusion System	86-11-31	FDA UDI	Class I	Active
Threshold V2 Pedicular Fixation System	10-10-83-12	FDA UDI	Class II	Active
Rampart One Lumbar Interbody Fusion System	10-10-76-35	FDA UDI	Class II	Active
SOAR Retractor System	78-02-45-3	FDA UDI	Class I	Active
Duo Expandable Interbody Fusion System	86-06-19-2	FDA UDI	Class I	Active
Duo Ti Expandable Interbody Fusion System	86-08-34	FDA UDI	Class I	Active
Fortress Pedicle Screw	10-10-49-3	FDA UDI	Class II	Unknown
Rampart-O	83-02-20-9	FDA UDI	Class II	Active
Fortress Pedicle Screw	10-10-48-39	FDA UDI	Class II	Unknown
OptiMesh Multiplanar Expandable Interbody Fusion System	32-30-08-2	FDA UDI	Class I	Active
CAPTURE Facet Screw Set System	70-02-012	FDA UDI	Class I	Active
Fortress Pedicale Screw	10-10-57-14	FDA UDI	Class II	Unknown
Rampart-T	83-01-06-8	FDA UDI	Class II	Active
Rampart-O	10-10-41-3	FDA UDI	Class II	Active
Rampart One Lumbar Interbody Fusion System	102-63-02	FDA UDI	Class II	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 16, 2024	Z-0117-2025	—	open, classified	Possible detachment of the Graft Tube shaft from the Graft Tube funnel head when it is not used as instructed by our surgical technique.