# Spirair, Inc.

- Location (FDA's records): South San Francisco, Ca
- FDA decisions: 5 (2023–2026): 5 510(k) clearances
- Product codes: NHB (4), LYA (1)
- Predicates its devices cite: 5 (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

## Firms whose devices it cites most
- Entrigue Surgical, Inc.: 1 (https://510kreport.com/company/entrigue-surgical)
- Spirox, Inc.: 1 (https://510kreport.com/company/spirox)

## Its most-cited devices
- K233569: SeptAlign (2024), cited by 1
- K251790: SeptAlign (2026), cited by 1
- K223167: Spirair Nasal Septal Strap (2023), cited by 1

## Recent decisions
- K260620: SeptAlign (SPLN001) (Jul 30, 2026)
- K251790: SeptAlign (Jan 16, 2026)
- K243655: TurbAlign (Jul 11, 2025)
- K233569: SeptAlign (Mar 22, 2024)
- K223167: Spirair Nasal Septal Strap (Aug 17, 2023)

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