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NANOVIS SPINE, LLC

US

Last updated September 17, 2026

What NANOVIS SPINE, LLC makes

Nanovis Spine, LLC manufactures spinal interbody fusion cages made from metal-polymer composites and polymers, as well as non-bioabsorbable spinal bone screws and fixation plates. Their product line includes devices like the FortiBridge, FortiCore Cervical Trial, and Nano FortiCore, designed for spinal stabilization and fusion procedures. The company also offers the Anatomic PEEK Cervical Fusion System with Nanotechnology, intended for cervical spine applications.

These devices are classified as Class II under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The company is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Nanovis Spine, LLC manufacture?

Nanovis Spine, LLC specializes in spinal devices used for stabilization and fusion. Their product line includes metal-polymer composite spinal interbody fusion cages, polymeric spinal interbody fusion cages, non-bioabsorbable spinal bone screws, and non-bioabsorbable spinal fixation plates. Examples include the FortiBridge, FortiCore Cervical Trial, and Nano FortiCore, which are designed for procedures requiring spinal support and fusion.

Where is Nanovis Spine, LLC based?

Nanovis Spine, LLC is headquartered in the United States. The company’s location is relevant for regulatory compliance and device distribution, as it operates within the FDA’s jurisdiction for device authorization.

Which regulatory registries list Nanovis Spine, LLC’s devices?

Nanovis Spine, LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for authorized devices, allowing healthcare providers and regulators to verify product details and compliance.

How are Nanovis Spine, LLC’s devices classified under FDA regulations?

Nanovis Spine, LLC’s devices fall under Class II classification by the FDA. This classification applies to devices that generally pose moderate risk and require special controls to ensure safety and effectiveness, such as spinal implants used for stabilization and fusion.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
5865 E State Road 14, Columbia City, IN, 46725
LinkedIn
—
Facebook
—
Phone
8779076266
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
3009446038
DUNS Number
079898044

Catalogue (644)

Page 5 of 13
DeviceModel / ReferenceRegistriesClassStatus
Anatomic PEEK™ Cervical Fusion System with Nanotechnology 6208764
FDA UDI
Class IIActive
FortiFix 12001-5555N
FDA UDI
Class IIActive
FortiBridge® 10703-4016
FDA UDI
Class IIActive
FortiFix 12005-8545N
FDA UDI
Class IIActive
FortiBridgeTM 10701-2032
FDA UDI
Class IIActive
Adaptix™ PEEK Interbody System with Nanotechnology 74332812
FDA UDI
Class IIActive
FortiBridge 10799-0010C
FDA UDI
Class IIActive
FortiCore® 11204-1610
FDA UDI
Class IIActive
FortiBridge® 10703-4012
FDA UDI
Class IIActive
FortiBridgeTM 10701-2036
FDA UDI
Class IIActive
FortiFix NV-908-1206
FDA UDI
Class IIActive
FortiBridgeTM 10708-4512
FDA UDI
Class IIActive
FortiFix 12005-5555N
FDA UDI
Class IIActive
FortiBridge 10711-3063
FDA UDI
Class IIActive
FortiBridge 10703-4018
FDA UDI
Class IIActive
Nano FortiCore® 11204-1612N
FDA UDI
Class IIActive
FortiBridgeTM 10703-4012
FDA UDI
Class IIActive
Nano FortiCore Cervical 11703-1408N
FDA UDI
Class IIActive
FortiBridgeTM 10701-3048
FDA UDI
Class IIActive
FortiCore® 11407-3211N
FDA UDI
Class IIActive
Adaptix™ PEEK Interbody System with Nanotechnology 74333409
FDA UDI
Class IIActive
FortiCore® 11302-2908N
FDA UDI
Class IIActive
FortiFix NV-908-1202
FDA UDI
Class IIActive
FortiBridge 10716-4016
FDA UDI
Class IIActive
FortiFix 12005-5545N
FDA UDI
Class IIActive
FortiFix 12005-6545N
FDA UDI
Class IIActive
Anatomic PEEK™ Cervical Fusion System with Nanotechnology 6208841
FDA UDI
Class IIActive
FortiBridge 10799-0012
FDA UDI
Class IIActive
FortiBridgeTM 10701-4101
FDA UDI
Class IIActive
FortiCore® 11407-3217N
FDA UDI
Class IIActive
FortiCore 10494-2808
FDA UDI
Class IIActive
FortiFix 12101-7560N
FDA UDI
Class IIActive
FortiBridgeTM 10701-2030
FDA UDI
Class IIActive
FortiCore 10494-2515
FDA UDI
Class IIActive
Nanovis Cervical FortiCore 11291-1606
FDA UDI
Class IIActive
FortiBridge® 10701-4081
FDA UDI
Class IIActive
FortiBridgeTM 10706-4014
FDA UDI
Class IIActive
FortiCore® 11403-2507
FDA UDI
Class IIActive
Adaptix™ PEEK Interbody System with Nanotechnology 74333415
FDA UDI
Class IIActive
Adaptix™ PEEK Interbody System with Nanotechnology 74332409
FDA UDI
Class IIActive
FortiFix 12005-8535N
FDA UDI
Class IIActive
FortiBridge 10799-0020
FDA UDI
Class IIActive
FortiFix NV-908-1204
FDA UDI
Class IIActive
FortiBridge® 10708-4514
FDA UDI
Class IIActive
FortiBridge® 10701-1020
FDA UDI
Class IIActive
FortiBridge 10799-0015
FDA UDI
Class IIActive
FortiBridgeTM 10701-4085
FDA UDI
Class IIActive
FortiCore 10494-2513
FDA UDI
Class IIActive
FortiCore® 11403-2515N
FDA UDI
Class IIActive
OrthoAccessTM 21502-3409
FDA UDI
Class IIActive

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