# Aoti, Ltd.

- Location (FDA's records): Galway, IE
- FDA decisions: 1 (2008–2008): 1 510(k) clearance
- Product codes: KPJ (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 1 (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
- Vascular One, Inc.: 1 (https://510kreport.com/company/vascular-one)
- Gwr Medical, Llp: 1 (https://510kreport.com/company/gwr-medical)
- Metro Medical Equipment, Inc.: 1 (https://510kreport.com/company/metro-medical-equipment)

## Firms that cite its devices most
- Vaporox, Inc.: 1 (https://510kreport.com/company/vaporox)

## Its most-cited devices
- K080966: Hyper-Box Topical Wound Oxygen System (2008), cited by 1

## Recent decisions
- K080966: Hyper-Box Topical Wound Oxygen System (Aug 6, 2008)

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