# Philips Consumer Lifestyle - Innovation Site Eindhoven

- Location (FDA's records): Eindhoven, NL
- FDA decisions: 3 (2016–2020): 3 510(k) clearances
- Product codes: HGX (3)
- 510(k) review time since 2016: median 88 days, against 128 for FDA's reviews in the same codes and years (2 of 3 faster)
- Predicates its devices cite: 3 (2 its own); citations of its devices by later devices: 3 (2 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: 1 (https://510kreport.com/company/medela)

## Firms that cite its devices most
- Avita Corporation: 1 (https://510kreport.com/company/avita)

## Its most-cited devices
- K201381: Philips Avent Single/Double electric breast pump Advanced (2020), cited by 2
- K161532: Philips Avent Comfort Single/Twin Electric Breast Pump (2016), cited by 1

## Recent decisions
- K203383: Philips Avent Double electric breast pump Advanced SCF394/61, Philips Avent Double electric breast pump Advanced SCF394/62 (Dec 15, 2020)
- K201381: Philips Avent Single/Double electric breast pump Advanced (Oct 1, 2020)
- K161532: Philips Avent Comfort Single/Twin Electric Breast Pump (Aug 29, 2016)

Source page: https://510kreport.com/company/philips-consumer-lifestyle-innovation-site-eindhoven