MOZO GRAU SA
ES-MF-000009479 · Spain · VALLADOLID
MOZO GRAU SA is registered in the European database on medical devices as a manufacturer, with 1 111 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIb | 789 |
|---|---|
| Class IIa | 322 |
Most frequent device types declared: DREXP, DRFID, DRILL, DRPRO, DRTAP.
Among these devices, 218 are declared sterile, 789 implantable, 80 reusable.
Devices declared under this manufacturer
- 1.25 hex retaining screw 2-3 mm Mini Inhex TCP
- 3,3x13 mm Grade IV Min TrC V2 Inhex Implant
- 3,3x15 mm Mini hybrid V2 Inhex Implant
- 3,75x15 mm Std hybrid Quattro Inhex Implant
- 30º Non hex Tap. abutment Maxi Inhex 5 mm
- 4,25x8 mm Std hybrid V2 Inhex Implant
- 5mm Hex str. abutment Std. Inhex 3 mm +screw
- Angled abutment retaining screw Mini Inhex
- Healing screw Std. Inhex 3 mm
- Hex str. abutment Mini Inhex 4 mm +screw TCP
- Hex str. abutment Mini Oss. 2 mm +screw
- Non hex titanium UCLA Maxi Oss. +screw
Showing 12 of 1 111 declared devices.
Catalogue references include 13207032, 23204830, 23207613, 232310151, 23604208, 23607043.
European nomenclature codes declared: P01020180, P01020101, Q010207, Q0199, L159007, Q019005.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | MOZO-GRAU SA (ES) · FDA 3031553803 |
| Devices in EUDAMED | 1 111 |
| Country of registration | Spain |
Device-level evidence
| Devices with a numeric GTIN | 1 111 |
|---|---|
| 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: United States only. MOZO GRAU SA is registered in the United States but was not found in the Canadian register.