# Neochild, LLC

- Location (FDA's records): Oklahoma City, OK
- FDA decisions: 1 (2009–2009): 1 510(k) clearance
- Product codes: KNT (1)
- Predicates its devices cite: 6 (0 its own); citations of its devices by later devices: 2 (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
- Promedic, Inc.: 2 (https://510kreport.com/company/promedic)
- Catco Medical, Inc.: 1 (https://510kreport.com/company/catco-medical)
- Gesco Intl., Inc.: 1 (https://510kreport.com/company/gesco-intl)
- Vygon Corp.: 1 (https://510kreport.com/company/vygon)
- Infusion Devices, Inc.: 1 (https://510kreport.com/company/infusion-devices)

## Firms that cite its devices most
- Benlan, Inc.: 1 (https://510kreport.com/company/benlan)
- Alan Reid: 1 (https://510kreport.com/company/alan-reid)

## Its most-cited devices
- K082710: Safechild Enteral Feeding Tube and Accessories and Feeding Tube Extension Set (2009), cited by 2

## Recent decisions
- K082710: Safechild Enteral Feeding Tube and Accessories and Feeding Tube Extension Set (Jan 23, 2009)

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