# Airxpanders, Inc.

- Location (FDA's records): Palo Alto, CA
- FDA decisions: 3 (2016–2019): 2 510(k) clearances and 1 De Novo grant
- Product codes: PQN (3)
- Predicates its devices cite: 2 (2 its own); citations of its devices by later devices: 2 (2 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
- K170075: AeroForm Tissue Expander (v3.0), AeroForm Dosage Controller (v1.5) (2017), cited by 1
- DEN150055: AeroForm Tissue Expander System (2016), cited by 1

## Recent decisions
- K191138: AeroForm Tissue Expander, Smooth (Jul 11, 2019)
- K170075: AeroForm Tissue Expander (v3.0), AeroForm Dosage Controller (v1.5) (Apr 3, 2017)
- DEN150055: AeroForm Tissue Expander System (Dec 21, 2016)

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