Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in FranceLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of SoproLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Sopro - Acteon Group with 4 510(k) clearances. The most recent is a 510(k) clearance dated Jun 17, 2016: S698 Symbioz flow.
| Jun 17, 2016 | S698 Symbioz flowK153367 · HIF | 510(k) clearances |
| Aug 17, 2015 | SOPIXK142995 · MUH | 510(k) clearances |
| Jul 31, 2015 | 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 scannerK151053 · MUH | 510(k) clearances |
| Sep 5, 2014 | SOPIX INSIDE, SOPIX2 INSIDEK140013 · MUH | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
