# Sonoscanner Sarl

- Location (FDA's records): Ivry Sur Seine, FR
- FDA decisions: 4 (2015–2024): 4 510(k) clearances
- Names in FDA's records: Sonoscanner Sarl (2); Sonoscanner (2)
- Product codes: IYN (4)
- 510(k) review time since 2016: median 105 days, against 83 for FDA's reviews in the same codes and years (0 of 3 faster)
- Predicates its devices cite: 4 (3 its own); citations of its devices by later devices: 3 (3 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
- GE Healthcare: 1 (https://510kreport.com/company/ge-healthcare)

## Its most-cited devices
- K143601: U-Lite (2015), cited by 1
- K171164: U-Lite EXP (2017), cited by 1
- K201988: T-Lite (2020), cited by 1

## Recent decisions
- K232285: U-Lite PRO (Jan 11, 2024)
- K201988: T-Lite (Oct 30, 2020)
- K171164: U-Lite EXP (Aug 3, 2017)
- K143601: U-Lite (Mar 18, 2015)

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