# Nanovis Spine, LLC

- Location (FDA's records): Columbia City, IN
- FDA decisions: 3 (2015–2020): 3 510(k) clearances
- Product codes: KWQ (2), NKB (1)
- Predicates its devices cite: 7 (1 its own); citations of its devices by later devices: 2 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Nanovis, LLC: 1 (https://510kreport.com/company/nanovis)
- Corelink, LLC: 1 (https://510kreport.com/company/corelink)
- Biomet Spine (Aka Ebi, LLC): 1 (https://510kreport.com/company/biomet-spine-aka-ebi)
- Medtronic Sofamor Danek USA, Inc.: 1 (https://510kreport.com/company/medtronic-sofamor-danek-usa)
- X-Spine Systems, Inc.: 1 (https://510kreport.com/company/x-spine-systems)
- Synthes (Usa): 1 (https://510kreport.com/company/synthes-usa)

## Firms that cite its devices most
- Nanovis, LLC: 1 (https://510kreport.com/company/nanovis)

## Its most-cited devices
- K193211: Nano FortiFix® System (2020), cited by 1
- K143706: FortiBridge Anterior Cervical Plate System (2015), cited by 1

## Recent decisions
- K193211: Nano FortiFix® System (Mar 20, 2020)
- K162250: FortiBridge Anterior Cervical Plate System (Oct 26, 2016)
- K143706: FortiBridge Anterior Cervical Plate System (Apr 10, 2015)

Source page: https://510kreport.com/company/nanovis-spine