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.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Trophy SAS with 15 510(k) clearances and 5 device recalls. The most recent is a device recall dated Jul 21, 2021: CS¿9600¿is¿an¿extraoral¿system¿intended¿to¿produce¿two-dimensional¿and¿three-dimensional….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jul 21, 2021 | CS¿9600¿is¿an¿extraoral¿system¿intended¿to¿produce¿two-dimensional¿and¿three-dimensional¿digital¿X-ray¿images¿of¿the¿dento-maxilofacial,¿ENTClass II · Device failed to function as intended and/or failed to conform to their design specifications. | Device recalls |
| Apr 2, 2020 | CS Model+K193390 · PNN | 510(k) clearances |
| Mar 13, 2020 | CS 9600K200183 · OAS | 510(k) clearances |
| May 24, 2018 | CS 9600K181136 · OAS | 510(k) clearances |
| Jan 16, 2018 | CS ImagingK173622 · LLZ | 510(k) clearances |
| Aug 21, 2015 | CS 8100SC, CS8100SC AccessK151087 · MUH | 510(k) clearances |
| Aug 19, 2015 | CS 3D ImagingK151837 · LLZ | 510(k) clearances |
| Sep 18, 2014 | DENTAL IMAGING SOFTWAREK141607 · LLZ | 510(k) clearances |
| Mar 14, 2014 | CS 8100 3DK133406 · OAS | 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
