# Incite Innovation, LLC

- Location (FDA's records): Springfield, MA
- FDA decisions: 4 (2010–2015): 4 510(k) clearances
- Names in FDA's records: Incite Innovation, LLC (3); Incite Innovation (1)
- Product codes: OVE (3), OVD (1)
- Predicates its devices cite: 8 (3 its own); citations of its devices by later devices: 5 (3 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
- Ldr Spine USA: 2 (https://510kreport.com/company/ldr-spine-usa)
- Synthes Spine: 1 (https://510kreport.com/company/synthes-spine)
- Biomet Spine: 1 (https://510kreport.com/company/biomet-spine)
- Zimmer Spine, Inc.: 1 (https://510kreport.com/company/zimmer-spine)

## Firms that cite its devices most
- Alphatec Spine, Inc.: 1 (https://510kreport.com/company/alphatec-spine)
- Nexus Spine, LLC: 1 (https://510kreport.com/company/nexus-spine)

## Its most-cited devices
- K122008: Incite Anchored Cervical Interbody (Aci) Fusion Device (2012), cited by 3
- K093808: Incite Innovation Stand Alone Interbody Fusion Device (2010), cited by 1
- K130306: Incite Anchored Cervical Interbody Device (2013), cited by 1

## Recent decisions
- K150913: Incite Anchored Cervical Interbody Device (Apr 30, 2015)
- K130306: Incite Anchored Cervical Interbody Device (Apr 11, 2013)
- K122008: Incite Anchored Cervical Interbody (Aci) Fusion Device (Nov 16, 2012)
- K093808: Incite Innovation Stand Alone Interbody Fusion Device (Mar 24, 2010)

Source page: https://510kreport.com/company/incite-innovation