Data / Medical devices / System, Image Processing, Radiological / France
FDA-registered makers of System, Image Processing, Radiological in France: 20 establishments
20 establishments in France are registered with the FDA to make System, Image Processing, Radiological (product code LLZ). 14 have a 510(k) clearance or PMA approval on file and 4 have a recall event. FDA data exported November 2, 2026.
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- Device
- System, Image Processing, Radiological
- Product code
- LLZ
- Country
- France
Makers of System, Image Processing, Radiological in France
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Ge Medical Systems SCS | Buc, France | Contract manufacturer, Manufacturer | 26 | April 21, 2025 | 0 | 2 | 0 | api.fda.gov |
| Olea Medical | La Ciotat Bouches-du-Rhone, France | Manufacturer | 7 | August 25, 2025 | 0 | 1 | 0 | api.fda.gov |
| S.M.A.I.O | SAINT-PRIEST Auvergne-Rhone-Alpes, France | Manufacturer | 3 | August 17, 2026 | 0 | 0 | 0 | api.fda.gov |
| Avatar Medical | paris Ile-de-France, France | Manufacturer | 2 | March 30, 2026 | 0 | 0 | 0 | api.fda.gov |
| Dosisoft | Cachan Ile-de-France, France | Manufacturer | 2 | March 14, 2025 | 0 | 0 | 0 | api.fda.gov |
| FH Industrie | QUIMPER Finistere, France | Manufacturer | 2 | September 30, 2022 | 0 | 0 | 0 | api.fda.gov |
| Therenva | Rennes Bretagne, France | Manufacturer | 2 | April 12, 2016 | 0 | 0 | 0 | api.fda.gov |
| Trophy | Marne La Vallee Ile-de-France, France | Manufacturer | 2 | January 16, 2018 | 0 | 0 | 0 | api.fda.gov |
| EOS imaging | Paris, France | Manufacturer | 1 | June 19, 2018 | 0 | 3 | 0 | api.fda.gov |
| Intelligence In Medical Technologies | Paris, France | Manufacturer | 1 | July 30, 2004 | 0 | 0 | 0 | api.fda.gov |
| Medecom | PLOUGASTEL DAOULAS Bretagne, France | Manufacturer | 1 | May 23, 2014 | 0 | 0 | 0 | api.fda.gov |
| Medicrea International | RILLIEUX-LA-PAPE Auvergne-Rhone-Alpes, France | Manufacturer, Specification developer | 1 | January 12, 2022 | 0 | 1 | 0 | api.fda.gov |
| Qynapse | Paris, France | Manufacturer | 1 | December 13, 2019 | 0 | 0 | 0 | api.fda.gov |
| Visible Patient Lab | Strasbourg Bas-Rhin, France | Manufacturer | 1 | November 5, 2021 | 0 | 0 | 0 | api.fda.gov |
| Blue Ortho | Meylan Isere, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Inheart | Pessac Gironde, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Koelis | MEYLAN Isere, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medtech SAS | MAUGUIO Occitanie, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rebrain | PESSAC Gironde, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Therapanacea | Paris, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.