Data / Medical devices / Spain / Mozo-Grau SA
Mozo-Grau SA: FDA-registered device maker in Valladolid, Spain, 1 510(k) clearance
Mozo-Grau SA is registered with the FDA (registration 3031553803) in Valladolid, Spain. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 16, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3031553803
- Address
- Santiago Lopez Gonzalez 7, Valladolid, Spain, 47197
- Owner or operator
- MOZO-GRAU SA (10090922)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- June 3, 2024
- Registered through
- 2026
- Brand names listed
- 0,9 Hex. C/a screwdriver L9 mm, 0.7 Dia. L9 mm Drill, 1 Dia. square C/a screwdriver L10 mm, 1,3 Dia. square C/a screwdriver L10 mm, 1.25 Hex. screwdr. for 7mm. dia. ratchet l. 14 mm, 1.25 Hex. screwdr. for 7mm. dia. ratchet l. 25 mm, 1.25 Hex. screwdr. for 7mm. dia. ratchet l. 8 mm, 1/4 size tray and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Abutment, Implant, Dental, Endosseous | NHA | 2 | Manufacturer | accessdata.fda.gov |
| Accessories, Implant, Dental, Endosseous | NDP | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Implant, Endosseous, Root-Form | DZE | 2 | Manufacturer | accessdata.fda.gov |
| Non-Irrigation Endosseous Dental Implant Drill Bits | QRQ | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| May 16, 2024 | K233137 | Ticare Dental Implant Systems | DZE | Substantially Equivalent | Mozograu S.A. | accessdata.fda.gov |
Compare with other makers
- All makers of Non-Irrigation Endosseous Dental Implant Drill Bits
- All makers of Implant, Endosseous, Root-Form
- All makers of Abutment, Implant, Dental, Endosseous
- All makers of Accessories, Implant, Dental, Endosseous
Updated May 16, 2024. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.