BACKBONE
FR-MF-000001874 · France · Le Bouscat
BACKBONE is registered in the European database on medical devices as a manufacturer, with 20 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 20 |
|---|
Most frequent device types declared: BB-LISA-2-220, BB-LISA-2-228, BB-LISA-2-260.
Among these devices, 16 are declared reusable.
Devices declared under this manufacturer
- LISA - Addiditional wrench
- LISA - Band forceps I
- LISA - Band forceps II
- LISA - Hook Wide
- LISA - Implant holder Size 10
- LISA - Implant holder Size 12
- LISA - Interlaminar Distractor
- LISA - Locker
- LISA - Tensionner
- LISA - Torque Limiting Connector
- LISA - Torque Limiting Handle
- LISA - Trial Spacer (Size 6)
Showing 12 of 20 declared devices.
Catalogue references include BB-LISA-2-206, BB-LISA-2-208, BB-LISA-2-214, BB-LISA-2-220, BB-LISA-2-226, BB-LISA-2-241.
European nomenclature codes declared: L091199,L1299, L091104,L1299, L091103,L1299, L090999,L1299, L0920,L1299, L1299,S010401.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 20 |
| 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 | 20 |
|---|---|
| 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. BACKBONE was not found in either the U.S. or the Canadian register.