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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 1 of 40

Device	Model / Reference	Registries	Class	Status
Rampart-O	83-02-44-12	FDA UDI	Class II	Active
Duo Ti Expandable Interbody Fusion System	86-12-03-1	FDA UDI	Class II	Active
Duo Ti Expandable Interbody Fusion System	86-12-03-12	FDA UDI	Class II	Active
Threshold Solid Pedicle Screw	10-10-78-36	FDA UDI	Class II	Active
Rampart-O	83-02-14-10	FDA UDI	Class II	Active
SOAR Retractor System	78-01-12	FDA UDI	Class I	Active
Elite Expandable Interbody Fusion System	35-04-04-1	FDA UDI	Class I	Active
Fortress Pedicale Screw	10-10-57-13	FDA UDI	Class II	Unknown
OptiLIF Endo, Direct Visualization System	102-31-04	FDA UDI	Class I	Active
Threshold V2 Pedicular Fixation System	102-67-01	FDA UDI	Class I	Active
Duo Ti Expandable Interbody Fusion System	86-11-23-14	FDA UDI	Class II	Active
Threshold Set Screww/ Pedicle Screw	10-10-09-X	FDA UDI	Class II	Active
Palisade Pedicular Fixation System	10-10-63-3	FDA UDI	Class II	Active
Threshold Pedicular Fixation System	53-02-10	FDA UDI	Class I	Active
Threshold Solid Pedicle Screw	10-10-78-14	FDA UDI	Class II	Active
OptiMesh Multiplanar Expandable Interbody Fusion System	102-64-01-3	FDA UDI	Class I	Active
Rampart One Lumbar Interbody Fusion System	49-03-01	FDA UDI	Class I	Active
Rampart-O	83-02-14-12	FDA UDI	Class II	Active
Duo Ti Expandable Interbody Fusion System	86-08-39	FDA UDI	Class I	Active
OptiMesh Expandable Interbody Fusion System	32-14-11	FDA UDI	Class II	Active
Diverted Bone Tube	102-11-100	FDA UDI	Class II	Unknown
SOAR Retractor System	78-01-01-3	FDA UDI	Class I	Active
Rampart One Lumbar Interbody Fusion Device	10-10-75-5	FDA UDI	Class II	Active
SOAR Retractor System	78-01-03-3	FDA UDI	Class I	Active
Rampart O	83-04-07-30	FDA UDI	Class II	Active
Fortress Rod	10-10-48-49	FDA UDI	Class II	Active
Rampart One Lumbar Interbody Fusion Device	10-10-75-6	FDA UDI	Class II	Active
VIA Spinous Process Fixation System	34-08-04	FDA UDI	Class II	Active
Universal Dilator	52-03-02	FDA UDI	Class I	Active
Duo Ti Expandable Interbody Fusion System	86-08-38	FDA UDI	Class I	Active
Duo Expandable Interbody Fusion System	86-06-14-5	FDA UDI	Class I	Active
Duo Ti Expandable Interbody Fusion System	86-11-09	FDA UDI	Class I	Active
Palisade Pedicular Fixation System	67-24-07	FDA UDI	Class I	Active
Rampart T Lumbar Interbody Fusion Device	10-10-72-9	FDA UDI	Class II	Unknown
SOAR Retractor System	78-02-01-1	FDA UDI	Class I	Active
Threshold Pedicle Screw	10-10-09-36	FDA UDI	Class II	Active
Navigation	16-02-01-1	FDA UDI	Class II	Active
Duo Ti Expandable Interbody Fusion System	86-08-35	FDA UDI	Class I	Active
Fortress Pedicle Screw	10-10-49-1	FDA UDI	Class II	Unknown
Threshold Solid Pedicle Screw	10-10-78-24	FDA UDI	Class II	Active
SOAR Retractor System	102-49-17	FDA UDI	Class I	Active
Fortress Pedicle Screw	10-10-48-2	FDA UDI	Class II	Active
Merlon Retractor System	19-01-17	FDA UDI	Class I	Active
Threshold V2 Reduction Screw	10-10-84-19	FDA UDI	Class II	Active
Rampart O	83-04-07-45	FDA UDI	Class II	Active
Rampart-O	83-02-10-9	FDA UDI	Class II	Active
Rampart-O	83-02-10-14	FDA UDI	Class II	Active
Medius Midline Retractor System	66-02-01-34	FDA UDI	Class I	Active
Threshold Pedicular Fixation System	53-17-02	FDA UDI	Class I	Active
Duo Ti Expandable Interbody Fusion System	86-12-02-4	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.