# Echolight S.P.A

- Location (FDA's records): Lecce, IT
- FDA decisions: 3 (2018–2022): 3 510(k) clearances
- Product codes: MUA (2), IYO (1)
- Predicates its devices cite: 7 (2 its own); citations of its devices by later devices: 2 (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
- Cyberlogic, Inc.: 1 (https://510kreport.com/company/cyberlogic)
- Beam-Med, Ltd.: 1 (https://510kreport.com/company/beam-med)
- Siemens Medical Solutions USA, Inc.: 1 (https://510kreport.com/company/siemens-medical-solutions-usa)
- General Electric Co.: 1 (https://510kreport.com/company/general-electric)
- Intelametrix, Inc.: 1 (https://510kreport.com/company/intelametrix)

## Its most-cited devices
- K180516: EchoS (2018), cited by 1
- K202514: EchoS Family (2021), cited by 1

## Recent decisions
- K212851: EchoSK and EchoSGyn modules for EchoS Family devices (Mar 16, 2022)
- K202514: EchoS Family (Feb 25, 2021)
- K180516: EchoS (Oct 19, 2018)

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