# Spiway, LLC

- Location (FDA's records): Carlsbad, CA
- FDA decisions: 4 (2014–2021): 4 510(k) clearances
- Product codes: LYA (4)
- Predicates its devices cite: 3 (3 its own); citations of its devices by later devices: 3 (3 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Its most-cited devices
- K180141: SPIWay Endonasal Access Guide (2018), cited by 1
- K153686: SPIWay Endonasal Access Guide (2016), cited by 1
- K132721: Spiway Endonasal Access Guide (2014), cited by 1

## Recent decisions
- K213153: SPIWay Endonasal Access Guide (Oct 27, 2021)
- K180141: SPIWay Endonasal Access Guide (Feb 16, 2018)
- K153686: SPIWay Endonasal Access Guide (Jan 28, 2016)
- K132721: Spiway Endonasal Access Guide (Jan 29, 2014)

Source page: https://510kreport.com/company/spiway