# Airon Corporation

- Location (FDA's records): Melbourne, FL
- FDA decisions: 4 (2003–2012): 4 510(k) clearances
- Product codes: CBK (3), BTL (1)
- Predicates its devices cite: 12 (4 its own); citations of its devices by later devices: 6 (4 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
- Pneupac, Ltd.: 2 (https://510kreport.com/company/pneupac)
- Bio-Med Devices, Inc.: 1 (https://510kreport.com/company/bio-med-devices)
- Smiths Medical International Ltd., Luton: 1 (https://510kreport.com/company/smiths-medical-international-luton)
- Sechrist Industries, Inc.: 1 (https://510kreport.com/company/sechrist-industries)
- A Plus Medical: 1 (https://510kreport.com/company/a-plus-medical)
- Emergency Medical Techology: 1 (https://510kreport.com/company/emergency-medical-techology)
- Caradyne, Ltd.: 1 (https://510kreport.com/company/caradyne)

## Firms that cite its devices most
- O-Two Medical Technologies, Inc.: 1 (https://510kreport.com/company/o-two-medical-technologies)
- Neoforce Group, Inc.: 1 (https://510kreport.com/company/neoforce-group)

## Its most-cited devices
- K043085: Modification to: Pneuton Ventilator (2004), cited by 2
- K024344: Pneuton Ventilator (2003), cited by 2
- K080692: Macs Cpap System (2008), cited by 2

## Recent decisions
- K121379: Pneuton Mini Ventilator Pneuton Mini Non-Invasive Ventilation (Niv) Kit Accessory (Oct 11, 2012)
- K080692: Macs Cpap System (Jun 20, 2008)
- K043085: Modification to: Pneuton Ventilator (Dec 20, 2004)
- K024344: Pneuton Ventilator (Jun 3, 2003)

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