Medbone Medical Devices
PT-MF-000016683 · Portugal · Linhó, Sintra
Medbone Medical Devices is registered in the European database on medical devices as a manufacturer, with 1 124 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class I | 1 124 |
|---|
Most frequent device types declared: FirstBone®BCP, FirstBone®TCP, Fusiongraft®BCP, Novoss®BCP, Novoss®TCP.
Among these devices, 1 124 are declared sterile, 1 124 implantable.
Devices declared under this manufacturer
- DentOss®TCP
- FirstBone®BCP
- FirstBone®TCP
- Fusiongraft®BCP
- Graftera®TCP
- Novoss®BCP
- Novoss®TCP
- Osseos®TCP
- Osteofit®BCP
- Osteofit®TCP
- QualyBone®BCP
- QualyBone®TCP
Showing 12 of 1 124 declared devices.
Catalogue references include BCP010505O, FBB142530W, FGB010520G, NVB152030B, OET010505P, OFB010510O.
European nomenclature codes declared: P900402.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 1 124 |
| Country of registration | Portugal |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 1 124 |
|---|---|
| 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. Medbone Medical Devices was not found in either the U.S. or the Canadian register.