# Avent America, Inc.

- Location (FDA's records): Framingham, MA
- FDA decisions: 4 (1994–2005): 4 510(k) clearances
- Product codes: HGX (2), HGY (1), HFS (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
- Medela AG: 2 (https://510kreport.com/company/medela)
- The First Years, Inc.: 1 (https://510kreport.com/company/first-years)

## Firms that cite its devices most
- Philips Electronics UK Limited: 1 (https://510kreport.com/company/philips-electronics-uk)

## Its most-cited devices
- K052047: Isis IQ Uno Handheld Electronic Breast Pump, Model 101 (2005), cited by 1

## Recent decisions
- K052047: Isis IQ Uno Handheld Electronic Breast Pump, Model 101 (Sep 22, 2005)
- K051413: Isis IQ Duo Twin Electronic Breast Pump, Model 100 (Aug 29, 2005)
- K952035: Niplette (Jul 28, 1995)
- K944117: Avent Nipple Shield (Oct 5, 1994)

Source page: https://510kreport.com/company/avent-america