Data / Medical devices / Abutment, Implant, Dental, Endosseous / Spain
FDA-registered makers of Abutment, Implant, Dental, Endosseous in Spain: 10 establishments
10 establishments in Spain are registered with the FDA to make Abutment, Implant, Dental, Endosseous (product code NHA). 5 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Abutment, Implant, Dental, Endosseous
- Product code
- NHA
- Country
- Spain
Makers of Abutment, Implant, Dental, Endosseous in Spain
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Terrats Medical, S.L. | Barbera del Valles Barcelona, Spain | Contract manufacturer, Manufacturer | 21 | June 9, 2026 | 0 | 0 | 0 | api.fda.gov |
| Talladium Espana, SL | LLEIDA Lerida, Spain | Contract manufacturer, Manufacturer | 8 | January 29, 2026 | 0 | 0 | 0 | api.fda.gov |
| Implant Protesis Dental 2004, S.L. | Premia de Dalt Barcelona, Spain | Manufacturer | 6 | January 22, 2026 | 0 | 0 | 0 | api.fda.gov |
| B.T.I. Biotechnology Institute, S.L. | Miñano Alava, Spain | Exporter to the US, Manufacturer, Specification developer | 5 | December 8, 2023 | 0 | 0 | 0 | api.fda.gov |
| Avinent Implant System S.L.U. | Santpedor Barcelona, Spain | Contract manufacturer, Manufacturer | 1 | October 24, 2013 | 0 | 0 | 0 | api.fda.gov |
| Biostar Laboratorios Slu | Pinto Madrid(Autonomous Community), Spain | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Gmi Dental Implantology, S.L. | Lleida Lerida, Spain | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mozo-Grau SA | Valladolid, Spain | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ziacom Implants Slu | Pinto Madrid(Province), Spain | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ZimVie Spain S.L.U. | Paterna Valencia(Province), Spain | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 2026. 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.