# Amplifon S.P.A.

- Location (FDA's records): Deer Field, IL
- FDA decisions: 8 (1997–1999): 8 510(k) clearances
- Product codes: EWO (4), ETY (2), GWF (2)
- Predicates its devices cite: 11 (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
- Amplus Corp.: 6 (https://510kreport.com/company/amplus)
- Amplaid USA, Inc.: 3 (https://510kreport.com/company/amplaid-usa)

## Firms that cite its devices most
- Amplaid: 1 (https://510kreport.com/company/amplaid)

## Its most-cited devices
- K971747: Amplaid 460 (1997), cited by 2
- K992370: Amplaid A724 and A728 (1999), cited by 1

## Recent decisions
- K992370: Amplaid A724 and A728 (Sep 20, 1999)
- K983915: Amplaid A315 and A319 (Jan 29, 1999)
- K983712: Amplaid A311 Series (Jan 12, 1999)
- K971740: Amplaid MK12 (Mar 16, 1998)
- K974235: Amplaid AM50 (Feb 10, 1998)
- K972959: Amplaid MK22 (Feb 6, 1998)
- K972862: Amplaid 171S (Oct 31, 1997)
- K971747: Amplaid 460 (Aug 5, 1997)

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