# Facetlink Dba Linkspine

- Location (FDA's records): Rockaway, NJ
- FDA decisions: 2 (2016–2017): 2 510(k) clearances
- Product codes: NKB (1), MAX (1)
- Predicates its devices cite: 6 (0 its own); citations of its devices by later devices: 2 (0 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
- Interpore Cross Intl.: 1 (https://510kreport.com/company/interpore-cross-intl)
- Aesculap, Inc.: 1 (https://510kreport.com/company/aesculap)
- Renovis Surgical Technologies, LLC: 1 (https://510kreport.com/company/renovis-surgical-technologies)
- Tyber Medical, LLC: 1 (https://510kreport.com/company/tyber-medical)
- Coalign Innovations, Inc.: 1 (https://510kreport.com/company/coalign-innovations)
- Eisertech, LLC: 1 (https://510kreport.com/company/eisertech)

## Firms that cite its devices most
- Linkspine, Inc.: 1 (https://510kreport.com/company/linkspine)
- Spine Smith Holdings, LLC: 1 (https://510kreport.com/company/spine-smith-holdings)

## Its most-cited devices
- K160722: CorticaLINK Spinal Fusion Platform (2016), cited by 2

## Recent decisions
- K162693: VertebraLINK Fusion Platform (Mar 29, 2017)
- K160722: CorticaLINK Spinal Fusion Platform (Jul 7, 2016)

Source page: https://510kreport.com/company/facetlink-dba-linkspine