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Sign in to claim this brandNANOVIS 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
- Website
- nanovistechnology.com
- —
- —
- [email protected]
- Phone
- 8779076266
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3009446038
- DUNS Number
- 079898044
Catalogue (644)
Page 3 of 13| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| FortiCore® | 11403-2807 | FDA UDI | Class II | Active |
| FortiBridge® | 10703-4014 | FDA UDI | Class II | Active |
| FortiCore | 10494-2510 | FDA UDI | Class II | Active |
| FortiCore® | 11407-3209N | FDA UDI | Class II | Active |
| FortiFix | 12101-8560N | FDA UDI | Class II | Active |
| Adaptix™ PEEK Interbody System with Nanotechnology | 74332411 | FDA UDI | Class II | Active |
| FortiCore® | 11204-1606 | FDA UDI | Class II | Active |
| FortiFix | 12001-8530N | FDA UDI | Class II | Active |
| FortiCore Cervical Trial | 11891-1609 | FDA UDI | Class II | Active |
| FortiCore® | 11403-2511 | FDA UDI | Class II | Active |
| FortiBridge® | 10708-4516 | FDA UDI | Class II | Active |
| FortiCore® | 11204-1611 | FDA UDI | Class II | Active |
| FortiBridge | 10711-1014 | FDA UDI | Class II | Active |
| FortiBridgeTM | 10701-2046 | FDA UDI | Class II | Active |
| Anatomic PEEK™ Cervical Fusion System with Nanotechnology | 3240886 | FDA UDI | Class II | Active |
| FortiFix | 12001-7535N | FDA UDI | Class II | Active |
| FortiCore® | 11403-2813 | FDA UDI | Class II | Active |
| FortiBridgeTM | 10701-4089 | FDA UDI | Class II | Active |
| FortiCore® | 11704-1607 | FDA UDI | Class II | Active |
| Anatomic PEEK™ Cervical Fusion System with Nanotechnology | 3200064 | FDA UDI | Class II | Active |
| FortiFix | 12001-6530N | FDA UDI | Class II | Active |
| FortiCore® | 11302-2912 | FDA UDI | Class II | Active |
| Nano FortiCore Cervical | 11703-1407N | FDA UDI | Class II | Active |
| Anatomic PEEK™ Cervical Fusion System with Nanotechnology | 3240086 | FDA UDI | Class II | Active |
| FortiBridge® | 10705-4514 | FDA UDI | Class II | Active |
| FortiBridge® | 10701-3063 | FDA UDI | Class II | Active |
| FortiCore® | 11403-2808N | FDA UDI | Class II | Active |
| Adaptix™ PEEK Interbody System with Nanotechnology | 74332416 | FDA UDI | Class II | Active |
| FortiCore® | 11302-3410N | FDA UDI | Class II | Active |
| FortiCore® | 11703-1408 | FDA UDI | Class II | Active |
| FortiBridge® | 10701-3060 | FDA UDI | Class II | Active |
| FortiCore Cervical Trial | 11892-1411 | FDA UDI | Class II | Active |
| FortiBridgeTM | 10701-2028 | FDA UDI | Class II | Active |
| FortiBridgeTM | 10701-4065 | FDA UDI | Class II | Active |
| FortiFix | 12101-8540N | FDA UDI | Class II | Active |
| FortiFix | NV-908-1208 | FDA UDI | Class II | Active |
| FortiFix | 12001-7540N | FDA UDI | Class II | Active |
| Adaptix™ PEEK Interbody System with Nanotechnology | 74332415 | FDA UDI | Class II | Active |
| FortiFix | 12005-7555N | FDA UDI | Class II | Active |
| FortiCore® | 11204-1612 | FDA UDI | Class II | Active |
| FortiCore | 10492-2210 | FDA UDI | Class II | Active |
| FortiCore® | 11407-3213 | FDA UDI | Class II | Active |
| FortiCore® | 11403-2517 | FDA UDI | Class II | Active |
| FortiBridge® | 10707-4016 | FDA UDI | Class II | Active |
| FortiBridge® | 10704-4018 | FDA UDI | Class II | Active |
| FortiBridge | 10711-2034 | FDA UDI | Class II | Active |
| FortiCore® | 11401-2212 | FDA UDI | Class II | Active |
| FortiFix | 12001-6550N | FDA UDI | Class II | Active |
| Anatomic PEEK™ Cervical Fusion System with Nanotechnology | 3240764 | FDA UDI | Class II | Active |
| Nanovis Cervical FortiCore | 11291-1607 | FDA UDI | Class II | Active |
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