JANTON (G2M)
FR-MF-000003877 · France · Saumur Cedex
JANTON (G2M) is registered in the European database on medical devices as a manufacturer, with 87 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 87 |
|---|
Most frequent device types declared: Accroches distales, Adjonction Accoudoir, Adjonction pour cale d'abduction, Adjonctions Têtières, Articulations de cheville avec vis à portée et démontable à clavette.
Devices declared under this manufacturer
- ACCROCHE DISTALE A PLONGEUR CREMAILLERE
- ADAPTATEUR PIED SACH STARFLEX
- ARTICUL.DE CHEVILLE INOX SF
- ARTICULATION OMEGA EXT GA
- Articulation Releveur
- Châssis Triskelo T1
- Châssis Triskelo T2
- Ensemble mentonnière droite
- Genou 4 axes aluminium
- Kit Triskelo T2
- PAIRE D'APPUI BRAS T2
- PIED ROYER ART.ANT&POST.BL 22D
Showing 12 of 87 declared devices.
Catalogue references include B21STFX, L10, PU4I-1EG, T67K-2, T8K-1, T90250A.
European nomenclature codes declared: Y99, Y061280, Y062499, Y1299, Y122406, Y122199.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 87 |
| Country of registration | France |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 87 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. JANTON (G2M) was not found in either the U.S. or the Canadian register.