ModJaw
FR-MF-000009804 · France · Villeurbanne
ModJaw is registered in the European database on medical devices as a manufacturer, with 8 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 8 |
|---|
Among these devices, 2 are declared active.
Devices declared under this manufacturer
- TWIN IN MOTION
Catalogue references include FORKS, NAVEX, SMILIT, TALLY, TIARA, TIARA2.
European nomenclature codes declared: Q0199.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | MODJAW (FR) · FDA 3014644422 |
| Devices in EUDAMED | 8 |
| Country of registration | France |
Device-level evidence
| Devices with a numeric GTIN | 8 |
|---|---|
| Found in the U.S. device database | 6 |
| Share | 75.0 % |
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: United States only. ModJaw is registered in the United States but was not found in the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
DZ 1379952-1 | issued | 2028-09-25 |