Tecnoss s.r.l.
IT-MF-000027289 · Italy · Torino
Tecnoss s.r.l. is registered in the European database on medical devices as a manufacturer, with 90 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class I | 90 |
|---|
Most frequent device types declared: Collagenated bone matrix, Collagenic membrane.
Among these devices, 90 are declared sterile, 90 implantable.
Devices declared under this manufacturer
- OsteoBiol® Apatos®
- OsteoBiol® Derma
- OsteoBiol® Evolution
- OsteoBiol® GTO®
- OsteoBiol® Gen-Os®
- OsteoBiol® Lamina®
- OsteoBiol® Sp-Block
- OsteoBiol® mp3®
- Tecnoss® Chips
- Tecnoss® Evolution
- Tecnoss® Gen-Os®
- Tecnoss® Lamina®
Showing 12 of 90 declared devices.
Catalogue references include ED75SS, EV04LLE, EVOHHE, M1005FE, M1005FS, M1010FE.
European nomenclature codes declared: P900402.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 90 |
| Country of registration | Italy |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 90 |
|---|---|
| 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. Tecnoss s.r.l. was not found in either the U.S. or the Canadian register.