# Sopro - Acteon Group

- Location (FDA's records): La Ciotat, FR
- FDA decisions: 4 (2014–2016): 4 510(k) clearances
- Product codes: MUH (3), HIF (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K153367: S698 Symbioz flow (Jun 17, 2016)
- K142995: SOPIX (Aug 17, 2015)
- K151053: PSPIX 2 scanner, Imaging Plate Size 0 for PSPIX2 scanner, Imaging Plate Size 1 for PSPIX2 scanner, Imaging Plate Size 2 for PSPIX2 scanner, Imaging Plate Size 3 for PSPIX2 scanner (Jul 31, 2015)
- K140013: Sopix Inside, SOPIX2 Inside (Sep 5, 2014)

Source page: https://510kreport.com/company/sopro-acteon-group